EP1963255A1 - Synephrine derivatives useful as anti-inflammatory agents - Google Patents

Synephrine derivatives useful as anti-inflammatory agents

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Publication number
EP1963255A1
EP1963255A1 EP06841157A EP06841157A EP1963255A1 EP 1963255 A1 EP1963255 A1 EP 1963255A1 EP 06841157 A EP06841157 A EP 06841157A EP 06841157 A EP06841157 A EP 06841157A EP 1963255 A1 EP1963255 A1 EP 1963255A1
Authority
EP
European Patent Office
Prior art keywords
chloride
group
synephrine
alkyl
compound according
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP06841157A
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German (de)
French (fr)
Inventor
Wim Vanden Berghe
Karolien De Bosscher
Serge Van Calenbergh
Guy Haegeman
Carl Jeffrey Lacey
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Universiteit Gent
Original Assignee
Universiteit Gent
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Publication date
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Publication of EP1963255A1 publication Critical patent/EP1963255A1/en
Withdrawn legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/06—Esters of carbamic acids
    • C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
    • C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C271/16—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by singly-bound oxygen atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C219/00—Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton
    • C07C219/26—Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton having esterified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
    • C07C219/28—Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton having esterified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton having amino groups bound to acyclic carbon atoms of the carbon skeleton
    • C07C219/30—Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton having esterified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton having amino groups bound to acyclic carbon atoms of the carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains further substituted by singly-bound oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Definitions

  • the present invention relates to novel synephrine derivatives being useful for treating or preventing inflammatory diseases or disorders.
  • the present invention also relates to a method for preparing such compounds, as well as to pharmaceutical compositions comprising a therapeutically effective amount of such compounds.
  • Synthetic glucocorticoids remain among the most effective agents for the treatment of chronic inflammatory diseases. However, major side effects severely limit their therapeutic use. Physiologic and therapeutic activities of glucocorticoids are mediated by a nuclear receptor belonging to a family of ligand-inducible transcription factors that, in addition to directly regulating their cognate gene programs, can also interfere with other signalling pathways, such as those using NF- ⁇ B.
  • NF- ⁇ B is an inducible transcription factor complex which regulates the expression of various genes involved in inflammatory and immune responses. It is activated upon exposure of cells to, among others, pro-inflammatory cytokines (such as TNF or IL-1 ), oxidants (such as hydrogen peroxide, ozone, superoxide anions), bacterial compounds, viral products, PKC activators (such as phorbol esters and platelet activating factor) and UV- or gamma-irradiation. NF- ⁇ B is therefore a promising target for anti-inflammatory and immuno- suppressive therapies. Inhibition of NF- ⁇ B activity by glucocorticoids has been well documented, although gene stimulatory effects by glucocorticoids have also been observed.
  • glucocorticoids remain among the most potent immuno-suppressive and anti-inflammatory drugs currently available, and are especially effective in the treatment of chronic asthma or rheumatoid arthritis
  • side effects such as hypothalamic-pituitary-adrenal axis insufficiency, diabetes, altered lipid metabolism, steroid myopathy, osteoporosis, and infectious or neuro-psychiatric complications significantly limit the therapeutic use of classical glucocorticoid agonists in a significant number of patients, especially patients having a predisposition to one or more of the above-stated disorders.
  • WO 01/45693 discloses 2-(4-acetoxyphenyl)-2-chloro-N-methylethyi- ammonium chloride as an anti-inflammatory agent. Therefore there is a regular need in the art for novel compounds having significant and specific anti-inflammatory properties without having the side- effects of known effective anti-inflammatory agents such as glucocorticoids. There is a regular need in the art for effective anti-inflammatory agents having improved metabolisation and/or pharmacokinetic behaviour and which therefore can be more easily formulated into effective dosage forms. There is also a need in the art for such novel compounds which can be easily produced in good yield and purity from commercially available materials through a limited number of fully reproducible synthetic process steps.
  • the present invention relates to the unexpected finding that certain synephrine derivatives having a specific substitution pattern are able to display specific anti-inflammatory activity.
  • this anti-inflammatory activity can be similar in extent as glucocorticoids.
  • An advantage of embodiments of the present invention is that this anti-inflammatory activity can be without having the significant side effects of glucocorticoids and other known antiinflammatory agents. These derivatives can be easily produced in good yield and purity from synephrine through a limited number of fully reproducible synthetic process steps.
  • the present invention therefore also relates to pharmaceutical compositions comprising a therapeutic effective amount of such synephrine derivatives, and optionally one or more pharmaceutically acceptable carriers.
  • the present invention also relates to the use of such synephrine derivatives for making a medicament for treating or preventing anti-inflammatory disorders (in particular chronic inflammatory diseases).
  • the present invention also includes a method of reduction or prevention or treatment of antiinflammatory disorders (in particular chronic inflammatory diseases) by the administration of synephrine derivatives to a patient in need thereof, optionally in combination with one or more other drugs such as, but not limited to, other anti-inflammatory agents.
  • this invention relates to such combinations having synergistic activity.
  • Figures 1A and 1 B show the performance of a representative compound of the present invention in an anti-inflammatory assay with comparison to reference compounds known in the art.
  • Figure 1A shows the anti-inflammatory activity of dexamethasone and of compound A.
  • Figure 1 B shows the anti-inflammatory effect of 1-[4-(benzoyloxy)phenyl]-2-[(terf- butoxycarbonyl)-methylamino]ethyl-1 H-imidazole-1 -carboxylate.
  • Figure 2 shows, according to an embodiment of the invention, the antiinflammatory activity of 1-[4-(naphthoyloxy)phenyl]-2-[(terf-butoxycarbonyl)- methylamino]ethyl-1 H-imidazole-1 -carboxylate.
  • Figure 3 shows, according to an embodiment of the invention, the antiinflammatory activity of 1-[4-(isobutanoyloxy)phenyl]-2-[(ferf-butoxycarbonyl)- methylamino]ethyl-1 H-imidazole-1 -carboxylate.
  • Ci -7 alkyl means straight and branched chain saturated acyclic hydrocarbon monovalent groups having from 1 to 7 carbon atoms such as, for example, methyl, ethyl, propyl, n-butyl, 1-methylethyl (isopropyl), 2-methylpropyl (isobutyl), 1 ,1- dimethylethyl (ter-butyl), 2-methylbutyl, n-pentyl, dimethylpropyl, n-hexyl, 2- methylpentyl, 3-methylpentyl, n-heptyl and the like; said Ci -7 alkyl group may further optionally include one or more suitable substituents independently selected from the group consisting of amino, halogen, hydroxy, sulfhydryl, trifluoromethyl, methoxy and the like.
  • C-2-io alkyl means straight and branched chain saturated acyclic hydrocarbon monovalent groups having from 2, 3, 4, 5, 6, 7, 8, 9 or 10 carbon atoms, such as but not limited to ethyl, propyl, n-butyl, 1-methylethyl (isopropyl), 2-methylpropyl (isobutyl), 1 ,1-dimethylethyl (ferf-butyl), 2-methylbutyl, n-pentyl, dimethylpropyl, n-hexyl, 2-methylpentyl, 3-methylpentyl, n-heptyl, n-octyl, n- nonyl, n-decyl and the like; said C 2- io alkyl group may further optionally include one or more suitable substituents independently selected from the group consisting of amino, halogen, hydroxy, sulfhydryl, trifluoromethyl,
  • cycloaliphatic and C- 3 - 10 cycloalkyl refer to a mono- or polycyclic saturated hydrocarbon monovalent group having from 3 to 10 carbon atoms, such as for instance cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl and the like, or a C 7- - I o polycyclic saturated hydrocarbon monovalent group having from 7 to 10 carbon atoms such as, for instance, norbornyl, fenchyl, trimethyltricycloheptyl or adamantyl.
  • C 3- io cycloalkyl-alkyl refers to an aliphatic saturated hydrocarbon monovalent group (preferably a Ci -7 alkyl such as defined above) to which a C 3- i 0 cycloalkyl (such as defined above) is already linked such as, but not limited to, cyclohexylmethyl, cyclopentylmethyl and the like.
  • aromatic and aryl designate any mono- or polycyclic aromatic monovalent hydrocarbon group having from 6 up to 30 carbon atoms such as but not limited to phenyl, naphthyl, anthracenyl, phenantracyl, fluoranthenyl, chrysenyl, pyrenyl, biphenylyl, terphenyl, picenyl, indenyl, biphenyl, indacenyl, benzocyclobutenyl, benzocyclooctenyl and the like, including fused cycloalkyl groups (the latter being as defined above) such as, for instance, indanyl, tetrahydronaphthyl, fluorenyl and the like, all of the said groups being optionally substituted with one or more substituents independently selected from the group consisting of halogen, amino, trifluoromethyl, hydroxyl, sulfhydryl and
  • heterocyclic means a mono- or polycyclic, saturated or mono-unsaturated or poly- unsaturated monovalent hydrocarbon group having from 2 up to 15 carbon atoms and including one or more heteroatoms in one or more rings, each of said rings having from 3 to 10 atoms (and optionally further including one or more heteroatoms attached to one or more carbon atoms of said ring, for instance in the form of a carbonyl or thiocarbonyl or selenocarbonyl group, and/or to one or more heteroatoms of said ring, for instance in the form of a sulfone, sulfoxide, N-oxide, phosphate, phosphonate or selenium oxide group), each of said heteroatoms being independently selected from the group consisting of nitrogen, oxygen, sulfur, selenium and phosphorus, also including groups wherein a heterocyclic ring is fused to one or more aromatic hydrocarbon rings for instance in the form of benzo-fused
  • Ci -7 alkoxy ", “C 3- io cycloalkoxy ", “ aryloxy “, “ arylalkyloxy “, “thio Ci -7 alkyl”, “ thio C3-10 cycloalkyl “, “ arylthio “ and “ arylalkylthio” refer to substituents wherein respectively a Ci -7 alkyl, a C 3- io cycloalkyl, aryl, arylalkyl or heterocyclic group (each of them such as defined herein), are attached to an oxygen atom or a divalent sulfur atom through a single bond, such as but not limited to methoxy, ethoxy, propoxy, butoxy, pentoxy, isopropoxy, sec-butoxy, tert-butoxy, isopentoxy, cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, thiomethyl, thioeth
  • halogen means any atom selected from the group consisting of fluoro, chloro, bromo and iodo.
  • C 2- 7 alkenyl designates a straight or branched acyclic hydrocarbon monovalent group having one or more ethylenic unsaturations and having from 2 to 7 carbon atoms such as, for example, vinyl, 1-propenyl, 2-propenyl (allyl), 1-butenyl, 2- butenyl, 2-pentenyl, 3-pentenyl, 3-methyl-2-butenyl, 3-hexenyl, 2-hexenyl, 2- heptenyl, 1 ,3-butadienyl, pentadienyl, hexadienyl, heptadienyl, heptatrienyl and the like.
  • arylalkyl refers to an aliphatic saturated or ethylenically unsaturated hydrocarbon monovalent group (preferably a Ci -7 alkyl or C 2 - 7 alkenyl such as defined above) onto which an aryl or heterocyclic group (such as defined above) is attached, and wherein the said aliphatic, aryl or heterocyclic group may be optionally substituted with one or more substituents independently selected from the group consisting of halogen, amino, hydroxyl, sulfhydryl, Ci -7 alkyl, trifluoromethyl and nitro, such as but not limited to benzyl, 4-chlorobenzyl, 4-fluorobenzyl, 2-fluorobenzyl, 3,4-dichlorobenzyl, 2,6-dichlorobenzyl, 3-methylbenzyl, 4-methylbenzy
  • alkylaryl and alkyl-substituted heterocyclic refer to an aryl or heterocyclic radical (such as defined above) onto which are bonded one or more aliphatic saturated or unsaturated hydrocarbon monovalent groups, preferably one or more Ci -7 alkyl, C 2-7 alkenyl or C 3- i 0 cycloalkyl groups as defined above such as, but not limited to, o-toluyl, m-toluyl, p-toluyl, 2,3-xylyl, 2,4-xylyl, 3,4-xylyl, o-cumenyl, m-cumenyl, p-cumenyl, o-cymenyl, m-cymenyl, p-cymenyl, mesityl, ter- butylphenyl, lutidinyl (i.e.
  • acyl refers to a substituent derived from an acid such as an organic monocarboxylic acid, a carbonic acid, a carbamic acid (resulting into a carbamoyl substituent) or the thioacid or imidic acid (resulting into a carbamidoyl substituent) corresponding to said acids
  • sulfonyl refers to a substituent derived from an organic sulfonic acid, wherein said acids comprise an aliphatic, aromatic or heterocyclic group in the molecule.
  • acyl group within the scope of the above definition refers to a carbonyl (oxo) group adjacent to a Ci -7 alkyl, a 0 3 .-10 cycloalkyl, an aryl, an arylalkyl or a heterocyclic group, all of them being such as herein defined. Suitable examples of acyl groups are to be found below.
  • Acyl and sulfonyl groups originating from aliphatic or cycloaliphatic monocarboxylic acids are designated herein as aliphatic or cycloaliphatic acyl and sulfonyl groups and include, but are not limited to, the following:
  • alkanoyl for example formyl, acetyl, propionyl, butyryl, isobutyryl, valeryl, isovaleryl, pivaloyl and the like;
  • cycloalkanoyl for example cyclobutanecarbonyl, cyclopentanecarbonyl, cyclohexanecarbonyl, 1-adamantanecarbonyl and the like;
  • cycloalkyl-alkanoyl for example cyclohexylacetyl, cyclopentylacetyl and the like
  • alkenoyl for example acryloyl, methacryloyl, crotonoyl and the like
  • alkylthioalkanoyl for example methylthioacetyl, ethylthioacetyl and the like
  • alkanesulfonyl for example mesyl, ethanesulfonyl, propanesulfonyl and the like
  • alkoxycarbonyl for example methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, isopropoxycarbonyl, butoxycarbonyl, isobutoxycarbonyl and the like;
  • alkylcarbamoyl for example methylcarbamoyl and the like
  • N-alkyl-thiocarbamoyl for example (N-methyl)-thiocarbamoyl and the like
  • alkylcarbamidoyl for example methylcarbamidoyl and the like
  • alkoxalyl for example methoxalyl, ethoxalyl, propoxalyl and the like
  • Acyl and sulfonyl groups may also originate from aromatic monocarboxylic acids and include, but are not limited to, the following:
  • - aroyl for example benzoyl, toluoyl, xyloyl, 1-naphthoyl, 2-naphthoyl and the like
  • - aralkanoyl for example phenylacetyl and the like
  • aryloxyalkanoyl for example phenoxyacetyl and the like
  • arylthioalkanoyl for example phenylthioacetyl and the like
  • arylaminoalkanoyl for example N-phenylglycyl, and the like
  • arylsulfonyl for example benzenesulfonyl, toluenesulfonyl, naphthalene sulfonyl and the like;
  • aryloxycarbonyl for example phenoxycarbonyl, naphthyloxycarbonyl and the like
  • arylcarbamoyl for example phenylcarbamoyl, naphthylcarbamoyl and the like
  • arylglyoxyloyl for example phenylglyoxyloyl and the like.
  • arylthiocarbamoyl for example phenylthiocarbamoyl and the like.
  • arylcarbamidoyl for example phenylcarbamidoyl and the like.
  • Acyl groups may also originate from an heterocyclic monocarboxylic acids and include, but are not limited to, the following:
  • heterocyclic-carbonyl in which said heterocyclic group is as defined herein, preferably an aromatic or non-aromatic 5- to 7-membered heterocyclic ring with one or more heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur in said ring (for example thiophenoyl, furoyl, pyrrolecarbonyl, nicotinoyl and the like);
  • heterocyclic-alkanoyl in which said heterocyclic group is as defined herein, preferably an aromatic or non-aromatic 5- to 7-membered heterocyclic ring with one or more heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur in said ring (for example thiopheneneacetyl, furylacetyl, imidazolylpropionyl, tetrazolylacetyl, 2-(2-amino-4-thiazolyl)-2- methoxyiminoacetyl and the like).
  • heterocyclic group is as defined herein, preferably an aromatic or non-aromatic 5- to 7-membered heterocyclic ring with one or more heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur in said ring (for example thiopheneneacetyl, furylacetyl, imidazolylpropionyl, tetrazolylacetyl, 2-(2-amino-4-thiazolyl)-2- meth
  • stereoisomer refers to all possible different isomeric as well as conformational forms which the compounds of this invention may possess, in particular all possible stereochemically and conformationally isomeric forms, all diastereomers, enantiomers and/or conformers of the basic molecular structure.
  • enantiomer means each individual optically active form of a compound of this invention, having an optical purity or enantiomeric excess (as may be determined by methods standard in the art) of at least 80% (i.e. at least 90% of one enantiomer and at most 10% of the other enantiomer), preferably at least 90% and more preferably at least 98%.
  • solvate includes any combination which may be formed by a derivative of this invention with a suitable inorganic solvent (e.g. hydrates) or organic solvent, such as but not limited to alcohols, ketones, esters and the like.
  • a suitable inorganic solvent e.g. hydrates
  • organic solvent such as but not limited to alcohols, ketones, esters and the like.
  • the present invention relates to a family of compounds represented by the structural formula (I):
  • R 4 is selected from the group consisting of R 5 , -OR 5 , -NHR 5 and -SR 5 ,
  • R 5 is selected from the group consisting of hydrogen; straight chain or branched chain, aliphatic or cycloaliphatic or aromatic groups such as C 2 - 10 alkyl, 02-10 alkenyl, C2-io cycloalkyl, C2-10 alkynyl, aryl, arylalkyl, and saturated, partly unsaturated or aromatic heterocyclic groups,
  • R 7 is C 1 -1 0 alkyl, C 2- io alkenyl, aryl, or aryl-Ci-i 0 alkyl, wherein each of said alkyl, alkenyl or aryl may be substituted with one or more substituents independently selected from the group consisting of halogen, alkyl, alkoxy, nitro, cyano and hydroxy, As well as stereoisomers thereof, solvates thereof, or salts thereof.
  • a first embodiment of this aspect of the invention relates to compounds wherein Ri is an acyl group derived from an aliphatic, cycloaliphatic, aromatic or heterocyclic monocarboxylic acid. Ri may be different from R 2 , especially when Ri is an aliphatic acyl group. Alternatively, according to a second embodiment of this aspect of the invention, when Ri is an acyl group derived from a cycloaliphatic, aromatic or heterocyclic monocarboxylic acid, Ri may be the same as R 2 .
  • a preferred embodiment of this aspect of the invention relates to compounds wherein Ri is selected from the group consisting of benzoyl, p-toluoyl, 1- naphthalenecarbonyl, 2-naphthalenecarbonyl, 4-morpholinocarbonyl, 1-piperi- dinocarbonyl, 1-imidazolidinocarbonyl, 1-pyrrolidinocarbonyl, 2-thiazole- carbonyl, 1-methyl-1 H-pyrrole-2-carbonyl, 2-furanecarbonyl, 3-furanecarbonyl, 3-pyridinecarbonyl, 4-pyridinecarbonyl, 2-thiophenecarbonyl, cyclobutane- carbonyl, cyclopentanecarbonyl, cyclohexanecarbonyl, 1-adamantane- carbonyl, pipecolinyl and 2-norbornanecarbonyl.
  • Ri is selected from the group consisting of benzoyl, p-toluoyl, 1- naphthalen
  • R 3 is the same as R 2 .
  • Suitable amino-protecting groups such as required for R 3 are well known in the art and are preferably selected from the group consisting of arylcarbonyl, alkyloxycarbonyl and arylalkyloxycarbonyl.
  • suitable amino-protecting groups include benzyloxycarbonyl (which may be introduced by reaction with benzylchloroformate under alkaline conditions, e.g. making use of sodium hydroxide or hydrogenocarbonate) and 9-fluorenylmethoxycarbonyl (which may be introduced by reaction with 9- fluorenylmethyl chloroformate).
  • amino-protecting group is a ferf-butoxycarbonyl group which may be introduced by reaction with di- tert-butyl dicarbonate under alcaline conditions.
  • suitable amino- protecting groups for R 3 include, but are not limited to aralkyl type protecting groups comprising benzyl, p-methoxybenzyl, p-nitrobenzyl, p-bromobenzyl and triphenylmethyl (trityl); alternative acyl type protecting groups comprising formyl, acetyl, chloroacetyl, dichloroacetyl, trichloroacetyl, trifluoroacetyl, phenylacetyl, o-nitrophenoxyacetyl, sec-butyryl, pivaloyl- (also known as tert- butyryl), cyclopropanoyl, benzoyl, o-nitrobenzoyl, and alpha-chlorobutyryl; or other urethane type protecting
  • Still another embodiment of the present invention relates to compounds represented by the structural formula (I), wherein a heterocyclic group Re may be attached through one of its heteroatoms to the carbon atom of the carbonyl group of R 2 .
  • the compound of the invention is present in the form of a non-toxic acid addition salt, more preferably a pharmaceutically acceptable acid addition salt, of a compound defined according to the above structural formula and wherein R 3 is hydrogen.
  • a non-toxic acid addition salt more preferably a pharmaceutically acceptable acid addition salt, of a compound defined according to the above structural formula and wherein R 3 is hydrogen.
  • the latter form includes any therapeutically active non-toxic addition salt which the compounds of this invention are able to form with a (preferably pharmaceutically acceptable) salt-forming agent.
  • Such addition salts may conveniently be obtained by treating the compounds of the invention with an effective amount (preferably an at least stoechiometric amount) of an appropriate salt-forming acid, while using reaction conditions (such as, but not limited to, temperature, pressure, time and the like) conventional in the art for such treatment.
  • compounds having basic properties such as the amino compounds of the present invention, may conveniently be converted into the corresponding therapeutically active, non-toxic acid addition salt form by treating the free base form with a suitable amount of an appropriate acid following conventional procedures.
  • appropriate salt-forming acids include, for instance, inorganic acids resulting in forming salts such as, but not limited to, hydrohalides (e.g.
  • hydrochloride and hydrobromide sulfate, nitrate, phosphate, diphosphate, carbonate, bicarbonate, and the like; and organic monocarboxylic or dicarboxylic acids resulting in forming salts such as, but not limited to, acetate, propanoate, hydroxyacetate, 2- hydroxypropanoate, 2-oxopropanoate, lactate, pyruvate, oxalate, malonate, succinate, maleate, fumarate, malate, tartrate, citrate, methanesulfonate, ethanesulfonate, benzoate, 2-hydroxybenzoate, 4-amino-2-hydroxybenzoate, benzene-sulfonate, p-toluenesulfonate, salicylate, p-aminosalicylate, pamoate, bitartrate, camphorsulfonate, edetate, 1 ,2-ethanedisulfonate, fumarate
  • An advantage of the present invention is that compounds defined according to the above structural formula are easily accessible in good yield and purity through a synthetic scheme involving a limited number of process steps and starting from commercially available materials.
  • An exemplary but non-limiting method for preparing the compounds of this invention comprises the steps of:
  • Carboxylic acid chlorides suitable for use in the synthesis of the compounds of the present invention include benzoyl chlorides such as, but not limited to, benzoyl chloride, p-anisoyl-chloride, 2-bromobenzoyl chloride, 4- bromobenzoyl chloride, 3-chlorobenzoyl chloride, pentafluorobenzoyl chloride, 2-chlorobenzoyl chloride, p-toluoyl chloride, 4-chlorobenzoyl chloride, 2,4- dichlorobenzoyl chloride, 3,4-dichlorobenzoyl chloride, 4-nitrobenzoyl chloride, 4-fluorobenzoyl chloride, 2-fluoro-benzoyl chloride, o-toluoyl chloride, m- toluoyl chloride, 4-cya no benzoyl chloride, 3-nitrobenzoyl chloride, 4-tert-butyl- benzoyl chloride, 4-
  • carboxylic acid chlorides are known to the person skilled in the art and commercially available for use as acylating reagent for use in the above reaction step.
  • Particular carbonyl chlorides for use in the method of the invention include, but are not limited to, cinnamoyl chloride, hydrocinnamoyl chloride, 2-phenylbutyryl chloride, phenylacetyl chloride and 4-fluorophenylacetyl chloride.
  • Phenylsulfonyl chlorides (represented by the structural formula V-B) suitable for use in the synthesis of the compounds of the present invention include, but are not limited to, 4-fluorobenzenesulfonyl chloride, 2- mesitylenesulfonyl chloride, 4-methoxybenzene-sulfonyl chloride, p- toluenesulfonyl chloride, pentafluorobenzene-sulfonyl chloride, benzenesulfonyl chloride, 4-bromobenzenesulfonyl chloride, N-acetylsulfanilyl chloride, 2,4,6-triisopropyl-benzenesulfonyl chloride 2- naphthalenesulfonylchloride, 4-chloro-benzenesulfonyl chloride 3,5-dichloro-2- hydroxy-benzenesulfonylchloride, 2,5-dich
  • Phenylacetyl chlorides also suitable for use in the synthesis of the compounds of the present invention include, but are not limited to, phenylacetyl chloride, 4-methoxyphenylacetyl chloride, 2-(2-naphthyl)acetyl chloride, 2-(3,5-difluorophenyl)ethanoyl chloride, 2-(1-naphthyl)ethanoyl chloride, 4-chlorophenylacetyl chloride, 3-methoxyphenylacetyl chloride, and 4-fluorophenylacetyl chloride.
  • the above method is able to provide compounds defined according to the above structural formula and wherein R 3 is an amino-protecting group such as referred herein above or, in the presence of an additional final step, wherein R 3 is hydrogen .
  • An exemplary but non-limiting embodiment of the method of the invention includes a step (a) comprising reacting synephrine with an amino-protected thiazolidine-2-thione.
  • the amino-protected thiazolidine-2-thione or other amino-protecting reagent may be dissolved in an organic solvent such as an ether for use in said step (a), and is preferably used in a molar ratio of at least 1 :1 , more preferably from 1 :1 to about 2:1 , with respect to synephrine.
  • step (a) is performed in a solvent system which may comprise water, a lower alcohol (such as, but not limited to, methanol), and optionally in the presence of a further organic solvent (such as the solvent used for introducing the amino-protected thiazolidine-2-thione or other amino-protecting reagent).
  • a solvent system which may comprise water, a lower alcohol (such as, but not limited to, methanol), and optionally in the presence of a further organic solvent (such as the solvent used for introducing the amino-protected thiazolidine-2-thione or other amino-protecting reagent).
  • a further organic solvent such as the solvent used for introducing the amino-protected thiazolidine-2-thione or other amino-protecting reagent.
  • step (b) said N-protected synephrine is reacted with a suitable chloride for introducing the relevant substituent R-i.
  • a suitable chloride for introducing the relevant substituent R-i.
  • Suitable experimental conditions for performing acylation or sulfonation step (b), especially the molar ratio between the selected acylating or sulfonating agent and the N-protected synephrine are well known in the art and, depending upon the selected acylating or sulfonating agent, and the number of hydroxyl groups to be acylated or sulfonated, may be tailored at will without undue experimentation.
  • step (c) said N-protected and acylated or sulfonated synephrine is reacted with a suitable activated carbonyl compound for introducing the relevant substituent R 2 .
  • Suitable experimental conditions for performing said step (c) are well known in the art and, depending upon the selected activated carbonyl compound, may be tailored at will without undue experimentation. It should be realized, however, that when R 2 is imidazolylcarbonyl or triazolylcarbonyl, a limited number of activated carbonyl compounds are available for efficiently introducing the substituent R 2 . In the latter situation, the activated carbonyl compound should preferably be carbonyldiimidazole or, respectively, carbonylditriazole, both being well known for their selective activation capacity.
  • the above-referred general synthetic method preferably further comprises a step (d) for selectively deprotecting the amino group of the compound resulting from step (c), without affecting any of groups Ri and R2 being present in said compound.
  • the amino- protecting group may be removed by deprotection methods conventional in the art, such as:
  • the method of said step (d) may be capable of simultaneously achieving selective deprotection of the amino group and the formation of a non-toxic acid addition salt such as, but not limited to, a hydrochloride, a hydrobromide or a trifluoroacetate, of the compounds of the invention wherein R 3 is hydrogen.
  • a non-toxic acid addition salt such as, but not limited to, a hydrochloride, a hydrobromide or a trifluoroacetate
  • the present invention relates to a pharmaceutical composition
  • a pharmaceutical composition comprising a therapeutic effective amount of a compound defined by the above structural formula (with any of the available individual meanings for each of R 1 , R 2 and R 3 ), and optionally one or more pharmaceutically acceptable carriers or excipients.
  • Said pharmaceutical composition may comprise a novel synephrine derivative of the invention as the single bio-active ingredient, or as a bio-active ingredient in combination with one or more other drugs in a combined preparation for a so-called combination therapy.
  • pharmaceutically acceptable carrier or excipient as used herein in relation to pharmaceutical compositions and combined preparations means any material or substance with which the bio-active principle(s), i.e. the synephrine derivative and the said one or more other drugs, may be formulated in order to facilitate application or dissemination to the locus to be treated, for instance by dissolving, dispersing or diffusing the said composition, and/or to facilitate its storage, transport or handling without impairing its effectiveness.
  • the pharmaceutically acceptable carrier may be a solid or a liquid or a gas which has been compressed to form a liquid, i.e. the compositions of this invention can suitably be used in the form of concentrates, emulsions, solutions, granulates, dusts, sprays, aerosols, pellets or powders, but are not limited thereto.
  • Suitable pharmaceutical carriers or excipients for use in the said pharmaceutical compositions and their formulation are well known to those skilled in the art. There is no particular restriction to their selection within the present invention although, in case of a low or very low water-solubility of the synephrine derivative of this invention, special attention must be paid to the selection of suitable carrier combinations that can assist in a proper formulation in view of the expected time release profile.
  • Suitable pharmaceutical carriers or excipients include additives such as, but not limited to, wetting agents, dispersing agents, stickers, adhesives, emulsifying or surface-active agents, thickening agents, complexing agents, gelling agents, solvents, coatings, antibacterial and antifungal agents (for example phenol, sorbic acid, chlorobutanol), isotonic agents (such as sugars or sodium chloride) and the like, provided that the same are consistent with standard pharmaceutical practice, i.e. carriers and additives which do not create severe and/or permanent damage to the mammal, in particular the human being, to be treated with said medicament.
  • additives such as, but not limited to, wetting agents, dispersing agents, stickers, adhesives, emulsifying or surface-active agents, thickening agents, complexing agents, gelling agents, solvents, coatings, antibacterial and antifungal agents (for example phenol, sorbic acid, chlorobutanol), isotonic agents (such as sugars or sodium chloride) and
  • compositions of the present invention may be prepared by any method well known in the art, for instance by homogeneously mixing, dissolving, spray-drying, coating and/or grinding the bio-active ingredient(s), in a one-step or a multi-steps procedure, with the selected carrier material(s) and, where appropriate, the other additives such as surface-active agents.
  • the pharmaceutical compositions of the present invention may also be prepared by micronisation, for instance in view to obtain them in the form of microspheres usually having a diameter of about 1 to about 10 ⁇ m, namely for the manufacture of microcapsules for controlled or sustained release of the said biologically-active ingredient(s).
  • Suitable surface-active agents useful as a pharmaceutically acceptable carrier or excipient in the pharmaceutical compositions of the present invention include non-ionic, cationic and/or anionic surfactants having good emulsifying, dispersing and/or wetting properties.
  • Suitable anionic surfactants include both water-soluble soaps and water-soluble synthetic surface-active agents.
  • Suitable soaps are alkaline or alkaline-earth metal salts, non- substituted or substituted ammonium salts of higher fatty acids (C10-C22). e.g. the sodium or potassium salts of oleic or stearic acid, or of natural fatty acid mixtures obtainable form coconut oil or tallow oil.
  • Synthetic surfactants include sodium or calcium salts of polyacrylic acids; fatty sulphonates and sulphates; sulphonated benzimidazole derivatives and alkylarylsulphonates.
  • Fatty sulphonates or sulphates are usually in the form of alkaline or alkaline-earth metal salts, non-substituted ammonium salts or ammonium salts substituted with an alkyl or acyl radical having from 8 to 22 carbon atoms, e.g.
  • Suitable sulphonated benzimidazole derivatives preferably contain 8 to 22 carbon atoms.
  • alkylarylsulphonates are the sodium, calcium or alcanolamine salts of dodecylbenzene sulphonic acid or dibutyl- naphtalenesulphonic acid or a naphtalene-sulphonic acid/formaldehyde condensation product.
  • corresponding phosphates e.g. salts of phosphoric acid ester and an adduct of p-nonylphenol with ethylene and/or propylene oxide, or phospholipids.
  • Suitable phospholipids for this purpose are the natural (originating from animal or plant cells) or synthetic phospholipids of the cephalin or lecithin type such as e.g.
  • phosphatidylethanolamine phosphatidylserine, phosphatidylglycerine, lysolecithin, cardiolipin, dioctanylphosphatidylcholine, dipalmitoylphoshatidyl- choline and their mixtures.
  • Suitable non-ionic surfactants useful as pharmaceutically acceptable carriers or excipients in the pharmaceutical compositions of the present invention include polyethoxylated and polypropoxylated derivatives of alkylphenols, fatty alcohols, fatty acids, aliphatic amines or amides containing at least 12 carbon atoms in the molecule, alkylarenesulphonates and dialkylsulphosuccinates, such as polyglycol ether derivatives of aliphatic and cycloaliphatic alcohols, saturated and unsaturated fatty acids and alkylphenols, said derivatives preferably containing 3 to 10 glycol ether groups and 8 to 20 carbon atoms in the (aliphatic) hydrocarbon moiety and 6 to 18 carbon atoms in the alkyl moiety of the alkylphenol.
  • non-ionic surfactants are water-soluble adducts of polyethylene oxide with poylypropylene glycol, ethylenediaminopolypropylene glycol containing 1 to 10 carbon atoms in the alkyl chain, which adducts contain 20 to 250 ethyleneglycol ether groups and/or 10 to 100 propyleneglycol ether groups.
  • Such compounds usually contain from 1 to 5 ethyleneglycol units per propyleneglycol unit.
  • non-ionic surfactants are nonylphenol-polyethoxyethanol, castor oil polyglycolic ethers, polypropylene/ polyethylene oxide adducts, tributylphenoxypolyethoxyethanol, polyethyleneglycol and octylphenoxypolyethoxyethanol.
  • Fatty acid esters of polyethylene sorbitan such as polyoxyethylene sorbitan trioleate
  • glycerol glycerol
  • sorbitan sucrose and pentaerythritol are also suitable non-ionic surfactants.
  • Suitable cationic surfactants useful as pharmaceutically acceptable carriers or excipients in the pharmaceutical compositions of the present invention include quaternary ammonium salts, preferably halides, having 4 hydrocarbon radicals optionally substituted with halo, phenyl, substituted phenyl or hydroxy; for instance quaternary ammonium salts containing as N- substituent at least one C ⁇ -C-22 alkyl radical (e.g. cetyl, lauryl, palmityl, myristyl, oleyl and the like) and, as further sub-stituents, unsubstituted or halogenated lower alkyl, benzyl and/or hydroxy-lower alkyl radicals.
  • quaternary ammonium salts preferably halides, having 4 hydrocarbon radicals optionally substituted with halo, phenyl, substituted phenyl or hydroxy
  • Structure-forming, thickening or gel-forming agents may be included into the pharmaceutical compositions and combined preparations of the invention.
  • Suitable such agents are in particular highly dispersed silicic acid, such as the product commercially available under the trade name Aerosil; bentonites; tetraalkyl ammonium salts of montmorillonites (e.g., products commercially available under the trade name Bentone), wherein each of the alkyl groups may contain from 1 to 20 carbon atoms; cetostearyl alcohol and modified castor oil products (e.g. the product commercially available under the trade name Antisettle).
  • Gelling agents which may be included into the pharmaceutical compositions and combined preparations of the present invention include, but are not limited to, cellulose derivatives such as carboxymethylcellulose, cellulose acetate and the like; natural gums such as arabic gum, xanthum gum, tragacanth gum, guar gum and the like; gelatin; silicon dioxide; synthetic polymers such as carbomers, and mixtures thereof.
  • Gelatin and modified celluloses represent a preferred class of gelling agents.
  • additives such as magnesium oxide; azo dyes; organic and inorganic pigments such as titanium dioxide; UV-absorbers; stabilisers; odor masking agents; viscosity enhancers; antioxidants such as, for example, ascorbyl palmitate, sodium bisulfite, sodium metabisulfite and the like, and mixtures thereof; preservatives such as, for example, potassium sorbate, sodium benzoate, sorbic acid, propyl gallate, benzylalcohol, methyl paraben, propyl paraben and the like; sequestering agents such as ethylene-diamine tetraacetic acid; flavoring agents such as natural vanillin; buffers such as citric acid and acetic acid; extenders or bulking agents such as silicates, diatomaceous earth, magnesium oxide or aluminum oxide; densification agents such as magnesium salts; and mixtures thereof.
  • additives such as magnesium oxide; azo dyes; organic and inorganic pigments such as titanium dioxide; UV-absorb
  • Control release compositions may thus be achieved by selecting appropriate polymer carriers such as for example polyesters, polyamino-acids, polyvinylpyrrolidone, ethylene-vinyl acetate copolymers, methylcellulose, carboxymethylcellulose, protamine sulfate and the like.
  • the rate of drug release and duration of action may also be controlled by incorporating the active ingredient into particles, e.g. microcapsules, of a polymeric substance such as hydrogels, polylactic acid, hydroxymethyl-cellulose, polymethyl methacrylate and the other above- described polymers.
  • Such methods include colloid drug delivery systems like liposomes, microspheres, microemulsions, nanoparticles, nanocapsules and so on.
  • the pharmaceutical composition or combined preparation of the invention may also require protective coatings.
  • Pharmaceutical forms suitable for injectable use include sterile aqueous solutions or dispersions and sterile powders for the extemporaneous preparation thereof.
  • Typical carriers or excipients for this purpose therefore include biocompatible aqueous buffers, ethanol, glycerol, propylene glycol, polyethylene glycol, complexing agents such as, but not limited to, cyclodextrins, maltodextrins and the like, and mixtures thereof.
  • this invention provides combinations, preferably synergistic combinations, of one or more synephrine derivatives represented by the above structural formula with one or more biologically-active drugs being preferably selected from the group consisting of anti-inflammatory drugs.
  • one or more biologically-active drugs being preferably selected from the group consisting of anti-inflammatory drugs.
  • this principle states that interactions (synergism, additivity, antagonism) between two drugs can be quantified using the combination index (hereinafter referred as Cl) defined by the following equation: a -E ⁇ L ED l c x " ED x la + ED/ 2 wherein ED x is the dose of the first or respectively second drug used alone (1a, 2a), or in combination with the second or respectively first drug (1c, 2c), which is needed to produce a given effect.
  • this principle may be applied to a number of desirable effects such as, but not limited to, an activity against inflammation.
  • the present invention relates to a pharmaceutical composition or combined preparation having synergistic effects against inflammation.
  • this invention provides the use of a synephrine derivative represented by the above structural formula (with any of the available individual meanings for each of R-i, R 2 and R 3 ) for the manufacture of a medicament for preventing or treating an inflammatory disease or disorder.
  • the compounds of the present invention have anti-inflammatory, analgesic and antipyretic activities comparable with glucocorticoids, but without side effects thereof, and are therefore safely useful in methods of treating or preventing diseases or conditions in which NF- ⁇ B and/or its target genes such as but not limited to IL-6, IL-8 and E-selectin are implicated.
  • Such diseases and conditions include, but are not limited to, those in which inflammation or tissue injury is involved such as osteoarthritis, rheumatoid arthritis, ankylosing spondilytis and the like, as well as other rheumatologic or pain indications.
  • Other diseases in which inflammation is involved and for which the novel compounds of the present invention are therapeutically useful include, but are not limited to, asthma, psoriasis, septic shock and inflammatory bowel disease. Since NF- ⁇ B may also be involved in apoptosis, the compounds of the present invention are also useful to limit tissue and/or cell damage and for ischaemic disease, neural injury or myocardial infarction.
  • the compounds of the invention are also useful in the treatment or prevention of Alzheimer's disease by delaying the onset or slowing the progression of said disease.
  • the aforementioned compounds of the invention may be administered by any conventional method including oral and parenteral (e. g. subcutaneous, intraperitoneal, intravascular or intramuscular) injection.
  • the treatment may consist of a single dose or a plurality of doses of the bio-active ingredient over a predetermined period of time.
  • the present invention involves a method of treating a patient having inflammation or an inflammation-related disorder by the administration of a therapeutically effective amount of a novel synephrine compound of the present invention.
  • the invention is therefore useful for, but not limited to, the treatment of inflammation in a patient, and for treatment of other inflammation- associated disorders such as pain, headache or fever.
  • the compounds of the present invention are also useful to treat arthritis, including but not limited to rheumatoid arthritis, spondylarthritis, gouty arthritis, osteoarthritis, systemic lupus erythematosus, and juvenile arthritis.
  • the compounds of the present invention are also useful in the treatment of asthma, bronchitis, menstrual cramps, tendinitis, bursitis, and skin-related conditions such as psoriasis, eczema, acne, burns and dermatitis.
  • the compounds of the present invention are useful for the treatment of gastrointestinal inflammatory conditions such as, but not limited to, inflammatory bowel disease, Crohn's disease, gastritis, irritable bowel syndrome and ulcerative colitis.
  • the compounds of the present invention are also useful in the treatment or prevention of inflammatory effects of cancer, such as colorectal cancer, breast cancer, prostate cancer or leukemia.
  • the compounds of the present invention are further useful in treating inflammation in diseases such as vascular diseases, migraine, headache, periarteritis nodosa, thyroiditis, plastic anemia, Hodgkin's disease, chroniclymphocytic leukemia, scleroderma, rheumatic fever, type I diabetes, myasthenia gravis, multiple sclerosis, sarcoidosis, nephrotic syndrome, Bechet's syndrome, polymyositis, gingivitis, myocardial ischemia and the like.
  • diseases such as vascular diseases, migraine, headache, periarteritis nodosa, thyroiditis, plastic anemia, Hodgkin's disease, chroniclymphocytic leukemia, scleroderma, rheumatic fever, type I diabetes, myasthenia gravis, multiple sclerosis, sarcoidosis, nephrotic syndrome, Bechet's syndrome, polymyositis, gingivitis, myo
  • the compounds of the present invention are useful in the treatment of inflammatory effects of ophthalmic diseases such as retinitis, retinopathy, conjunctivitis, uveitis, ocular photophobia, and acute injury to the eye tissue.
  • ophthalmic diseases such as retinitis, retinopathy, conjunctivitis, uveitis, ocular photophobia, and acute injury to the eye tissue.
  • the compounds of the present invention are also useful in the treatment of pulmonary inflammation, such as one associated with viral infection or cystic fibrosis.
  • the compounds of the present invention are further useful for the treatment of certain central nervous system disorders such as, but not limited to, cortical dementia, Alzheimer's disease, and multiple sclerosis.
  • the compounds of the present invention are also useful in the treatment of allergic rhinitis, respiratory distress syndrome, endotoxin shock syndrome, atherosclerosis and central nervous system damage resulting from stroke, ischemia or trauma.
  • the compounds of the present invention are also useful for the treatment
  • the term "therapeutally-effective" as used herein refers to an amount of the bio-active agent for use in anti-inflammation therapy which achieves improvement in inflammation severity, as may be determined by any practical or reproducible method.
  • the pharmaceutical composition of this invention may be in the form of a dosage unit containing a predetermined amount of the bio-active ingredient. Examples of such dosage units are tablets or capsules.
  • the therapeutically active amount of compound that can be administered and the dosage regimen for treating an inflammatory disease condition with a compound and/or pharmaceutical composition of this invention depends on a variety of factors, including the age, weight, sex and medical condition of the patient, the severity of the disease, the route and frequency of administration, and the particular compound used, and thus may vary in accordance with said factors.
  • the pharmaceutical composition may contain the bio-active ingredient of this invention in a range from about 0.1 to about 2000 mg, preferably about 0.5 to 500 mg and more preferably about 1 to 100 mg per dosage unit.
  • a daily dose of about 0.01 to 100 mg/kg body weight, preferably about 0.1 to 20 mg/kg body weight and more preferably about 0.1 to 10 mg/kg body weight, may be appropriate for administration to a human being.
  • the daily dose may suitably be administered in one to four sub-doses per day.
  • R., -alkyl, -aryl, -o-alkyl, -o-aryl
  • EXAMPLE 1 preparation of a N-protected svnephrine The following refers to the preparation of N-protected synephrines according to scheme 1 , step a.
  • Synephrine (referred as 13 in the above scheme 1 ) (1.65 g, 9.87 mmol) was dissolved in a boiling mixture of water (25 ml) and methanol (12 ml). This hot solution was stirred vigorously, and then a yellow solution of a N-acyl thiazolidine-2-thione (referred to as 14 in the above scheme 1 ; for the purpose of the present example N-acetyl-thiazolidine-2-thione (14a) was used) (1.592 g, 9.87 mmol) in THF (10 ml) was added portion-wise.
  • 14 in the above scheme 1 for the purpose of the present example N-acetyl-thiazolidine-2-thione (14a) was used
  • N-Boc-thiazolidine-2- thione may be easily obtained by reacting di-terf-butyl dicarbonate with 1 ,3- thiazolidine-2-thione preferably in the presence of an organic base such as triethylamine.
  • N-Boc thiazolidine-2-thione was added to a boiling solution of synephrine in methanol and water followed by one molar equivalent of triethyl amine. The solution was maintained at 7O 0 C.
  • the crude resulting product was purified by column chromatography using a mixture of CH 2 CI 2 and MeOH in a volume to volume ratio of 98:2, to yield 85% of the pure crystalline material.
  • reaction flask was chilled in an ice bath, and addition of 0.25 equivalent of triethylamine followed by drop-wise addition of 0.25 equivalent of the same acyl chloride was carried out. After one hour, thin layer chromatography (TLC) analysis (performed with a 98:2 (volume ratio) ChbCVmethanol mixture indicated that reaction was complete.
  • the reaction solution was diluted with methylene chloride and extracted with a half- saturated NaHC ⁇ 3 solution. The organic layer was dried over anhydrous MgSO 4 , filtered and concentrated into an oil.
  • the crude material obtained was purified by column chromatography (100 g silica gel, 98:2 (volume ratio) CH 2 Cl 2 /methanol mixture) to afford the desired product with a yield of about 70%.
  • N-BOC synephrine as obtained in example 2 (1.75 mmole) dissolved in 6 ml methanol was added solid potassium hydroxide (85 mg, 1.516 mmole). The mixture was stirred until full KOH dissolution, then methanol was removed under reduced pressure. The resulting residue was dried under vacuum, placed under a nitrogen atmosphere and then stirred in 3 ml of dry DMF. Once dissolution was effected, an acyl chloride such as benzoyl chloride (1.516 mmole) was added drop-wise so that only slight warming was observed.
  • an acyl chloride such as benzoyl chloride (1.516 mmole) was added drop-wise so that only slight warming was observed.
  • EXAMPLE 12 preparation of 4-M-(acetyloxy)-2-(methylamino)ethvHphenyl acetate hydrochloride
  • the following refers to the preparation of di-O-acyLsynephrine salts according to scheme 1 , step f.
  • a compound obtained according to example 2 (0.246 mmol) was dissolved in 1 ml of 4M HCI in dioxane, and the resulting solution was stirred at room temperature for 1 hour.
  • TLC analysis performed with a 98:2 (volume ratio) ChbCVmethanol mixture) after one hour indicated complete disappearance of the starting material.
  • L929sA cells were cultured in DMEM supplemented with 5 % new-born calf serum and 5 % fetal calf serum, 100 units/ml penicillin and 0.1 mg/ml streptomycin.
  • L929sA mouse fibroblast cells were stably transfected with pE- selectine-Luc (also referred to as pELAM-luc) by the calcium phosphate precipitation procedure described by De Bosscher et al. in Proc. Natl. Acad. Sci. USA (1997) 94:13504-13509.
  • L929sA cells were transiently transfected by the DEAE-dextran transfection method described by De Bosscher et al. (cited supra).
  • Recombinant murine tumor necrosis factor (TNF) was produced according to a method standard in the art.
  • DEX Dexamethasone
  • compound A 2-(4-acetoxyphenyl)-2-chloro- N-methyl-ethylammonium chloride
  • Induction was performed in triplicate for each independent experiment, which was carried out at least twice.
  • Induction with DEX compound A 1 and for the compound of example 6 according to this invention at 1 ⁇ M, 10 ⁇ M or respectively any other indicated concentration were performed at - 2 hours for a total of 8 hours, while TNF (2000 IU/ml) was added at time point zero and left on the cells for 6 hours.
  • TNF 2000 IU/ml
  • cells were lysed with a lysis buffer (commercially available from Tropix, Bedford, Massachussets) and samples were assayed according to the manufacturer's instructions (Promega Biotech). Promoter activities are expressed as a ratio of luciferase over ⁇ - galactosidase, multiplied by 100.
  • L929sA mouse fibroblast cells were cultured in DMEM supplemented with 5% newborn calf serum and 5% FCS, 100 units/ml penicillin and 0.1 mg/ml streptomycin.
  • the L929sA mouse fibroblast cells were stably transfected with plasmid p(IL6-kB) 3 -50hu.ll_6P-luc+ by a calcium phosphate precipitation procedure wel known in the art.
  • TNF, Dexamethasone, and compound A were obtained and handled as described for example 13.
  • Inductions were performed in triplicate for each independent experiment, which was carried out at least twice. Inductions with DEX, compound A or synephrine derivatives of the present invention at 1mM, 1OmM or at the indicated concentrations respectively, were performed at -2 hours for a total of 8 hours, while TNF (20001 U/ml) was added at time point zero and left on the cells for 6 hours.
  • Synephrine derivatives tested according to this protocol included 1-[4-(isobutanoyloxy)phenyl]-2-[(ferNbutoxycarbonyl)-methyl-amino]- ethyl-1 H-imidazole-1-carboxylate, and 1-[4-(naphthoyloxy)phenyl]-2-[(fe/t- butoxycarbonyl)-methylamino]ethyl-1 H-imidazole-1 -carboxylate.
  • TNF 1 cells After induction with TNF 1 cells were lysed with a lysis buffer (commercially available from TROPIX, Bedford, Massachussets) and samples were assayed for their protein or ⁇ -galactosidase content and luciferase activity according to the manufacturer's instructions (Promega Biotech). Promoter activities are calculated as ratios of luciferase over ⁇ -galactosidase and represented as ' induction fold ', whereby the promoter activity of the solvent-treated fraction was arbitrarily taken as 1.
  • synephrine derivatives are antiinflammatory agents, and that their mechanism of action is directed at the transcriptional level of NF-kB-driven genes (with NF-kB being widely acknowledged as a key regulatory transcription factor driving inflammatory cytokine gene expression), we tested the recombinant NF-kB-driven promoter construct p(IL6-kB) 3 -50hu.lL6P-luc+, stably integrated into L929sA cells, and observed for specific and selected synephrine derivatives an inhibition of the pro-inflammatory TNF-induced gene expression in a dose-responsive manner.
  • Figure 2 illustrates the anti-inflammatory effect of 1-[4-(naphthoyloxy)- phenyll ⁇ -Kte/t-butoxycarbonylJ-methylaminolethyl-I H-imidazole-i-carboxy- late (referred to in figure 2 as Naphth).
  • Figure 3 illustrates the antiinflammatory effect of 1-[4-(isobutanoyloxy)phenyl]-2-[(fe/t-butoxycarbonyl)- methylamino]ethyl-1 H-imidazole-1-carboxylate (referred to in figure 3 as Isobut).
  • Dexamethasone and compound A referred to in figure 2 and 3 as DEX and CpdA respectively
  • DEX and CpdA solvent control
  • synephrine derivatives of this invention display a marked anti-inflammatory potential.
  • the anti-inflammatory effectiveness of the active compounds are comparable to the effectiveness obtained by using known anti-inflammatory compounds such as dexamethasone or compound A.

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Abstract

This invention provides compounds having the structural formula: wherein:- R1 is an acyl or sulfonyl group, - R2 is an acyl group selected from the group consisting of acyl groups derived from cycloaliphatic, aromatic or heterocyclic monocarboxylic acids, imidazolylcarbonyl and triazolylcarbonyl, and - R3 is hydrogen or an amino-protecting group, a stereoisomer thereof, a solvate thereof, or a salt thereof, being useful as anti-inflammatory agents.

Description

SYNEPHRINE DERIVATIVES USEFUL AS ANTI-INFLAMMATORY AGENTS
Field of the invention
The present invention relates to novel synephrine derivatives being useful for treating or preventing inflammatory diseases or disorders. The present invention also relates to a method for preparing such compounds, as well as to pharmaceutical compositions comprising a therapeutically effective amount of such compounds.
Background of the invention
Synthetic glucocorticoids remain among the most effective agents for the treatment of chronic inflammatory diseases. However, major side effects severely limit their therapeutic use. Physiologic and therapeutic activities of glucocorticoids are mediated by a nuclear receptor belonging to a family of ligand-inducible transcription factors that, in addition to directly regulating their cognate gene programs, can also interfere with other signalling pathways, such as those using NF-κB.
NF-κB is an inducible transcription factor complex which regulates the expression of various genes involved in inflammatory and immune responses. It is activated upon exposure of cells to, among others, pro-inflammatory cytokines (such as TNF or IL-1 ), oxidants (such as hydrogen peroxide, ozone, superoxide anions), bacterial compounds, viral products, PKC activators (such as phorbol esters and platelet activating factor) and UV- or gamma-irradiation. NF-κB is therefore a promising target for anti-inflammatory and immuno- suppressive therapies. Inhibition of NF-κB activity by glucocorticoids has been well documented, although gene stimulatory effects by glucocorticoids have also been observed. Although glucocorticoids remain among the most potent immuno-suppressive and anti-inflammatory drugs currently available, and are especially effective in the treatment of chronic asthma or rheumatoid arthritis, side effects such as hypothalamic-pituitary-adrenal axis insufficiency, diabetes, altered lipid metabolism, steroid myopathy, osteoporosis, and infectious or neuro-psychiatric complications significantly limit the therapeutic use of classical glucocorticoid agonists in a significant number of patients, especially patients having a predisposition to one or more of the above-stated disorders.
WO 01/45693 discloses 2-(4-acetoxyphenyl)-2-chloro-N-methylethyi- ammonium chloride as an anti-inflammatory agent. Therefore there is a regular need in the art for novel compounds having significant and specific anti-inflammatory properties without having the side- effects of known effective anti-inflammatory agents such as glucocorticoids. There is a regular need in the art for effective anti-inflammatory agents having improved metabolisation and/or pharmacokinetic behaviour and which therefore can be more easily formulated into effective dosage forms. There is also a need in the art for such novel compounds which can be easily produced in good yield and purity from commercially available materials through a limited number of fully reproducible synthetic process steps.
Summary of the invention
The present invention relates to the unexpected finding that certain synephrine derivatives having a specific substitution pattern are able to display specific anti-inflammatory activity. In accordance with some embodiments of the present invention this anti-inflammatory activity can be similar in extent as glucocorticoids. An advantage of embodiments of the present invention is that this anti-inflammatory activity can be without having the significant side effects of glucocorticoids and other known antiinflammatory agents. These derivatives can be easily produced in good yield and purity from synephrine through a limited number of fully reproducible synthetic process steps.
The present invention therefore also relates to pharmaceutical compositions comprising a therapeutic effective amount of such synephrine derivatives, and optionally one or more pharmaceutically acceptable carriers. The present invention also relates to the use of such synephrine derivatives for making a medicament for treating or preventing anti-inflammatory disorders (in particular chronic inflammatory diseases). The present invention also includes a method of reduction or prevention or treatment of antiinflammatory disorders (in particular chronic inflammatory diseases) by the administration of synephrine derivatives to a patient in need thereof, optionally in combination with one or more other drugs such as, but not limited to, other anti-inflammatory agents. In particular, this invention relates to such combinations having synergistic activity.
Brief description of the drawings
Figures 1A and 1 B show the performance of a representative compound of the present invention in an anti-inflammatory assay with comparison to reference compounds known in the art. Figure 1A shows the anti-inflammatory activity of dexamethasone and of compound A. Figure 1 B shows the anti-inflammatory effect of 1-[4-(benzoyloxy)phenyl]-2-[(terf- butoxycarbonyl)-methylamino]ethyl-1 H-imidazole-1 -carboxylate.
Figure 2 shows, according to an embodiment of the invention, the antiinflammatory activity of 1-[4-(naphthoyloxy)phenyl]-2-[(terf-butoxycarbonyl)- methylamino]ethyl-1 H-imidazole-1 -carboxylate.
Figure 3 shows, according to an embodiment of the invention, the antiinflammatory activity of 1-[4-(isobutanoyloxy)phenyl]-2-[(ferf-butoxycarbonyl)- methylamino]ethyl-1 H-imidazole-1 -carboxylate.
Definitions
As used herein, and unless otherwise stated, the term " Ci-7 alkyl " means straight and branched chain saturated acyclic hydrocarbon monovalent groups having from 1 to 7 carbon atoms such as, for example, methyl, ethyl, propyl, n-butyl, 1-methylethyl (isopropyl), 2-methylpropyl (isobutyl), 1 ,1- dimethylethyl (ter-butyl), 2-methylbutyl, n-pentyl, dimethylpropyl, n-hexyl, 2- methylpentyl, 3-methylpentyl, n-heptyl and the like; said Ci-7 alkyl group may further optionally include one or more suitable substituents independently selected from the group consisting of amino, halogen, hydroxy, sulfhydryl, trifluoromethyl, methoxy and the like. As used herein, and unless otherwise stated, the term " C-2-io alkyl " means straight and branched chain saturated acyclic hydrocarbon monovalent groups having from 2, 3, 4, 5, 6, 7, 8, 9 or 10 carbon atoms, such as but not limited to ethyl, propyl, n-butyl, 1-methylethyl (isopropyl), 2-methylpropyl (isobutyl), 1 ,1-dimethylethyl (ferf-butyl), 2-methylbutyl, n-pentyl, dimethylpropyl, n-hexyl, 2-methylpentyl, 3-methylpentyl, n-heptyl, n-octyl, n- nonyl, n-decyl and the like; said C2-io alkyl group may further optionally include one or more suitable substituents independently selected from the group consisting of amino, halogen, hydroxy, sulfhydryl, trifluoromethyl, methoxy and the like.
As used herein, and unless otherwise stated, the terms " cycloaliphatic " and " C-3-10 cycloalkyl " refer to a mono- or polycyclic saturated hydrocarbon monovalent group having from 3 to 10 carbon atoms, such as for instance cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl and the like, or a C7--Io polycyclic saturated hydrocarbon monovalent group having from 7 to 10 carbon atoms such as, for instance, norbornyl, fenchyl, trimethyltricycloheptyl or adamantyl.
As used herein, the term " C3-io cycloalkyl-alkyl " refers to an aliphatic saturated hydrocarbon monovalent group (preferably a Ci-7 alkyl such as defined above) to which a C3-i0 cycloalkyl (such as defined above) is already linked such as, but not limited to, cyclohexylmethyl, cyclopentylmethyl and the like.
As used herein, and unless otherwise stated, the terms " aromatic " and " aryl " designate any mono- or polycyclic aromatic monovalent hydrocarbon group having from 6 up to 30 carbon atoms such as but not limited to phenyl, naphthyl, anthracenyl, phenantracyl, fluoranthenyl, chrysenyl, pyrenyl, biphenylyl, terphenyl, picenyl, indenyl, biphenyl, indacenyl, benzocyclobutenyl, benzocyclooctenyl and the like, including fused cycloalkyl groups (the latter being as defined above) such as, for instance, indanyl, tetrahydronaphthyl, fluorenyl and the like, all of the said groups being optionally substituted with one or more substituents independently selected from the group consisting of halogen, amino, trifluoromethyl, hydroxyl, sulfhydryl and nitro, such as for instance 4-fluorophenyl, 4-chlorophenyl, 3,4- dichlorophenyl, 4-cyanophenyl, 2,6-dichlorophenyl, 2-fluorophenyl, 3- chlorophenyl, 3,5-dichlorophenyl and the like.
As used herein, and unless otherwise stated, the term " heterocyclic " means a mono- or polycyclic, saturated or mono-unsaturated or poly- unsaturated monovalent hydrocarbon group having from 2 up to 15 carbon atoms and including one or more heteroatoms in one or more rings, each of said rings having from 3 to 10 atoms (and optionally further including one or more heteroatoms attached to one or more carbon atoms of said ring, for instance in the form of a carbonyl or thiocarbonyl or selenocarbonyl group, and/or to one or more heteroatoms of said ring, for instance in the form of a sulfone, sulfoxide, N-oxide, phosphate, phosphonate or selenium oxide group), each of said heteroatoms being independently selected from the group consisting of nitrogen, oxygen, sulfur, selenium and phosphorus, also including groups wherein a heterocyclic ring is fused to one or more aromatic hydrocarbon rings for instance in the form of benzo-fused, dibenzo-fused or naphto-fused heterocyclic groups; within this definition are included heterocyclic groups such as, but not limited to, diazepinyl, oxadiazinyl, thiadiazinyl, dithiazinyl, triazolonyl, diazepinonyl, triazepinyl, triazepinonyl, tetrazepinonyl, benzoquinolinyl, benzothiazinyl, benzothiazinonyl, benzoxa- thiinyl, benzodioxinyl, benzodithiinyl, benzoxazepinyl, benzothiazepinyl, benzodiazepinyl, benzodioxepinyl, benzodithiepinyl, benzoxazocinyl, benzothiazocinyl, benzodiazocinyl, benzoxathiocinyl, benzo-dioxocinyl, benzotrioxepinyl, benzoxathiazepinyl, benzoxadiazepinyl, benzothia- diazepinyl, benzotriazepinyl, benzoxathiepinyl, benzotriazinonyl, benzoxazolinonyl, azetidinonyl, azaspiroundecyl, dithiaspirodecyl, selenazinyl, selenazolyl, selenophenyl, hypoxanthinyl, azahypoxanthinyl, bipyrazinyl, bipyridinyl, oxazolidinyl, diselenopyrimidinyl, benzodioxocinyl, benzopyrenyl, benzopyranonyl, benzophenazinyl, benzoquinolizinyl, dibenzocarbazolyl, dibenzoacridinyl, dibenzophenazinyl, dibenzothiepinyl, dibenzooxepinyl, dibenzopyranonyl, dibenzoquinoxalinyl, dibenzothiazepinyl, dibenzoiso- quinolinyl, tetraazaadamantyl, thiatetraazaadamantyl, oxauracil, oxazinyl, dibenzothiophenyl, dibenzofuranyl, oxazolinyl, oxazolonyl, azaindolyl, azolonyl, thiazolinyl, thiazolonyl, thiazolidinyl, thiazanyl, pyrimidonyl, thiopyrimidonyl, thiamorpholinyl, azlactonyl, naphtindazolyl, naphtindolyl, naphtothiazolyl, naphtothioxolyl, naphtoxindolyl, naphtotriazolyl, naphto- pyranyl, oxabicycloheptyl, azabenzimidazolyl, azacycloheptyl, azacyclooctyl, azacyclononyl, azabicyclononyl, tetrahydrofuryl, tetrahydropyranyl, tetrahydro- pyronyl, tetrahydroquinoleinyl, tetrahydrothienyl and dioxide thereof, dihydrothienyl dioxide, dioxindolyl, dioxinyl, dioxenyl, dioxazinyl, thioxanyl, thioxolyl, thiourazolyl, thiotriazolyl, thiopyranyl, thiopyronyl, coumarinyl, quinoleinyl, oxyquinoleinyl, quinuclidinyl, xanthinyl, dihydropyranyl, benzo- dihydrofuryl, benzothiopyronyl, benzothiopyranyl, benzoxazinyl, benzoxazolyl, benzodioxolyl, benzodioxanyl, benzothiadiazolyl, benzotriazinyl, benzo- thiazolyl, benzoxazolyl, phenothioxinyl, phenothiazolyl, phenothienyl (benzothiofuranyl), phenopyronyl, phenoxazolyl, pyridinyl, dihydropyridinyl, tetrahydropyridinyl, piperidinyl, morpholinyl, thiomorpholinyl, pyrazinyl, pyrimidinyl, pyridazinyl, triazinyl, tetrazinyl, triazolyl, benzotriazolyl, tetrazolyl, imidazolyl, pyrazolyl, thiazolyl, thiadiazolyl, isothiazolyl, oxazolyl, oxadiazolyl, pyrrolyl, furyl, dihydrofuryl, furoyl, hydantoinyl, dioxolanyl, dioxolyl, dithianyl, dithienyl, dithiinyl, thienyl, indolyl, indazolyl, benzofuryl, quinolyl, quinazolinyl, quinoxalinyl, carbazolyl, phenoxazinyl, phenothiazinyl, xanthenyl, purinyl, benzothienyl, naphtothienyl, thianthrenyl, pyranyl, pyronyl, benzopyronyl, isobenzofuranyl, chromenyl, phenoxathiinyl, indolizinyl, quinolizinyl, isoquinolyl, phthalazinyl, naphthiridinyl, cinnolinyl, pteridinyl, carbolinyl, acridinyl, perimidinyl, phenanthrolinyl, phenazinyl, phenothiazinyl, imidazolinyl, imidazolidinyl, benzimidazolyl, pyrazolinyl, pyrazolidinyl, pyrrolinyl, pyrrolidinyl, piperazinyl, uridinyl, thymidinyl, cytidinyl, azirinyl, aziridinyl, diazirinyl, diaziridinyl, oxiranyl, oxaziridinyl, dioxiranyl, thiiranyl, azetyl, dihydroazetyl, azetidinyl, oxetyl, oxetanyl, oxetanonyl, homopiperazinyl, homopiperidinyl, thietyl, thietanyl, diazabicyclooctyl, diazetyl, diaziridinonyl, diaziridinethionyl, chromanyl, chromanonyl, thiochromanyl, thiochromanonyl, thiochromenyl, benzofuranyl, benzisothiazolyl, benzo-carbazolyl, benzochromonyl, benziso- alloxazinyl, benzocoumarinyl, thiocoumarinyl, phenometoxazinyl, phenoparoxazinyl, phentriazinyl, thiodiazinyl, thiodiazolyl, indoxyl, thioindoxyl, benzodiazinyl (e.g. phtalazinyl), phtalidyl, phtalimidinyl, phtalazonyl, alloxazinyl, dibenzopyronyl (i.e. xanthonyl), xanthionyl, isatyl, isopyrazolyl, isopyrazolonyl, urazolyl, urazinyl, uretinyl, uretidinyl, succinyl, succinimido, benzylsultimyl, benzylsultamyl and the like, including all possible isomeric forms thereof, wherein each carbon atom of said heterocyclic ring may be independently substituted with a substituent selected from the group consisting of halogen, nitro, Ci-7 alkyl (such as above defined, in particular methyl), C3-7 alkenyl, trifluoromethyl, C3-10 cycloalkyl, aryl, arylalkyl, alkylaryl, hydroxyl, sulfhydryl, Ci-7 alkoxy (such as above defined, in particular methoxy), aryloxy, arylalkyloxy, thio Ci-7 alkyl, thio C3-i0 cycloalkyl, thioaryl, arylalkylthio, cyano, carboxylic acid or esters thereof; depending upon the number of unsaturations in each of said rings, heterocyclic groups may be sub-divided into heteroaromatic (or " heteroaryl") groups and non-aromatic heterocyclic groups; when a heteroatom of the said non-aromatic heterocyclic group is nitrogen, the latter may be substituted with a substituent selected from the group consisting of Ci-7 alkyl, C3-IO cycloalkyl, aryl, arylalkyl and alkylaryl (each of said groups being as defined herein).
As used herein, and unless otherwise stated, the terms " Ci-7 alkoxy ", "C3-io cycloalkoxy ", " aryloxy ", " arylalkyloxy ", "thio Ci-7 alkyl", " thio C3-10 cycloalkyl ", " arylthio " and " arylalkylthio " refer to substituents wherein respectively a Ci-7 alkyl, a C3-io cycloalkyl, aryl, arylalkyl or heterocyclic group (each of them such as defined herein), are attached to an oxygen atom or a divalent sulfur atom through a single bond, such as but not limited to methoxy, ethoxy, propoxy, butoxy, pentoxy, isopropoxy, sec-butoxy, tert-butoxy, isopentoxy, cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, thiomethyl, thioethyl, thiopropyl, thiobutyl, thiopentyl, thiocyclopropyl, thiocyclobutyl, thiocyclopentyl, thiophenyl, phenyloxy, benzyloxy, mercaptobenzyl, cresoxy, and the like.
As used herein, and unless otherwise stated, the term " halogen " means any atom selected from the group consisting of fluoro, chloro, bromo and iodo.
As used herein, and unless otherwise stated, the term " C2-7 alkenyl " designates a straight or branched acyclic hydrocarbon monovalent group having one or more ethylenic unsaturations and having from 2 to 7 carbon atoms such as, for example, vinyl, 1-propenyl, 2-propenyl (allyl), 1-butenyl, 2- butenyl, 2-pentenyl, 3-pentenyl, 3-methyl-2-butenyl, 3-hexenyl, 2-hexenyl, 2- heptenyl, 1 ,3-butadienyl, pentadienyl, hexadienyl, heptadienyl, heptatrienyl and the like. As used herein, and unless otherwise stated, the terms " arylalkyl ", " arylalkenyl " and " heterocyclic-substituted alkyl " refer to an aliphatic saturated or ethylenically unsaturated hydrocarbon monovalent group (preferably a Ci-7 alkyl or C2-7 alkenyl such as defined above) onto which an aryl or heterocyclic group (such as defined above) is attached, and wherein the said aliphatic, aryl or heterocyclic group may be optionally substituted with one or more substituents independently selected from the group consisting of halogen, amino, hydroxyl, sulfhydryl, Ci-7 alkyl, trifluoromethyl and nitro, such as but not limited to benzyl, 4-chlorobenzyl, 4-fluorobenzyl, 2-fluorobenzyl, 3,4-dichlorobenzyl, 2,6-dichlorobenzyl, 3-methylbenzyl, 4-methylbenzyl, 4-ter- butylbenzyl, phenylpropyl, 1-naphthylmethyl, phenylethyl, 1-amino-2- phenylethyl, 1 -amino-2-[4-hydroxy-phenyl]ethyl, 1 -amino-2-[indol-2-yl]ethyl, styryl, pyridylmethyl (including all isomers thereof), pyridylethyl, 2-(2- pyridyl)isopropyl, oxazolylbutyl, 2-thienylmethyl, pyrrolylethyl, morpholinylethyl, imidazol-1-yl-ethyl, benzodioxolylmethyl and 2-furylmethyl.
As used herein, and unless otherwise stated, the term " alkylaryl " and " alkyl-substituted heterocyclic " refer to an aryl or heterocyclic radical (such as defined above) onto which are bonded one or more aliphatic saturated or unsaturated hydrocarbon monovalent groups, preferably one or more Ci-7 alkyl, C2-7 alkenyl or C3-i0 cycloalkyl groups as defined above such as, but not limited to, o-toluyl, m-toluyl, p-toluyl, 2,3-xylyl, 2,4-xylyl, 3,4-xylyl, o-cumenyl, m-cumenyl, p-cumenyl, o-cymenyl, m-cymenyl, p-cymenyl, mesityl, ter- butylphenyl, lutidinyl (i.e. dimethylpyridyl), 2-methylaziridinyl, methyl- benzimidazolyl, methylbenzofuranyl, methylbenzothiazolyl, methylbenzo- triazolyl, methylbenzoxazolyl and methylbenzselenazolyl.
As used herein, and unless otherwise stated, the term " acyl " refers to a substituent derived from an acid such as an organic monocarboxylic acid, a carbonic acid, a carbamic acid (resulting into a carbamoyl substituent) or the thioacid or imidic acid (resulting into a carbamidoyl substituent) corresponding to said acids, and the term " sulfonyl " refers to a substituent derived from an organic sulfonic acid, wherein said acids comprise an aliphatic, aromatic or heterocyclic group in the molecule. A more specific kind of " acyl " group within the scope of the above definition refers to a carbonyl (oxo) group adjacent to a Ci-7 alkyl, a 03.-10 cycloalkyl, an aryl, an arylalkyl or a heterocyclic group, all of them being such as herein defined. Suitable examples of acyl groups are to be found below.
Acyl and sulfonyl groups originating from aliphatic or cycloaliphatic monocarboxylic acids are designated herein as aliphatic or cycloaliphatic acyl and sulfonyl groups and include, but are not limited to, the following:
- alkanoyl (for example formyl, acetyl, propionyl, butyryl, isobutyryl, valeryl, isovaleryl, pivaloyl and the like);
- cycloalkanoyl (for example cyclobutanecarbonyl, cyclopentanecarbonyl, cyclohexanecarbonyl, 1-adamantanecarbonyl and the like);
- cycloalkyl-alkanoyl (for example cyclohexylacetyl, cyclopentylacetyl and the like);
- alkenoyl (for example acryloyl, methacryloyl, crotonoyl and the like);
- alkylthioalkanoyl (for example methylthioacetyl, ethylthioacetyl and the like);
- alkanesulfonyl (for example mesyl, ethanesulfonyl, propanesulfonyl and the like);
- alkoxycarbonyl (for example methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, isopropoxycarbonyl, butoxycarbonyl, isobutoxycarbonyl and the like);
- alkylcarbamoyl (for example methylcarbamoyl and the like);
- (N-alkyl)-thiocarbamoyl (for example (N-methyl)-thiocarbamoyl and the like);
- alkylcarbamidoyl (for example methylcarbamidoyl and the like); and - alkoxalyl (for example methoxalyl, ethoxalyl, propoxalyl and the like);
Acyl and sulfonyl groups may also originate from aromatic monocarboxylic acids and include, but are not limited to, the following:
- aroyl (for example benzoyl, toluoyl, xyloyl, 1-naphthoyl, 2-naphthoyl and the like); - aralkanoyl (for example phenylacetyl and the like);
- aralkenoyl (for example cinnamoyl and the like);
- aryloxyalkanoyl (for example phenoxyacetyl and the like);
- arylthioalkanoyl (for example phenylthioacetyl and the like); - arylaminoalkanoyl (for example N-phenylglycyl, and the like);
- arylsulfonyl (for example benzenesulfonyl, toluenesulfonyl, naphthalene sulfonyl and the like);
- aryloxycarbonyl (for example phenoxycarbonyl, naphthyloxycarbonyl and the like);
- aralkoxycarbonyl (for example benzyloxycarbonyl and the like);
- arylcarbamoyl (for example phenylcarbamoyl, naphthylcarbamoyl and the like);
- arylglyoxyloyl (for example phenylglyoxyloyl and the like). - arylthiocarbamoyl (for example phenylthiocarbamoyl and the like); and
- arylcarbamidoyl (for example phenylcarbamidoyl and the like).
Acyl groups may also originate from an heterocyclic monocarboxylic acids and include, but are not limited to, the following:
- heterocyclic-carbonyl, in which said heterocyclic group is as defined herein, preferably an aromatic or non-aromatic 5- to 7-membered heterocyclic ring with one or more heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur in said ring (for example thiophenoyl, furoyl, pyrrolecarbonyl, nicotinoyl and the like);
- heterocyclic-alkanoyl in which said heterocyclic group is as defined herein, preferably an aromatic or non-aromatic 5- to 7-membered heterocyclic ring with one or more heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur in said ring (for example thiopheneneacetyl, furylacetyl, imidazolylpropionyl, tetrazolylacetyl, 2-(2-amino-4-thiazolyl)-2- methoxyiminoacetyl and the like). As used herein and unless otherwise stated, the term " stereoisomer " refers to all possible different isomeric as well as conformational forms which the compounds of this invention may possess, in particular all possible stereochemically and conformationally isomeric forms, all diastereomers, enantiomers and/or conformers of the basic molecular structure. As used herein and unless otherwise stated, the term " enantiomer " means each individual optically active form of a compound of this invention, having an optical purity or enantiomeric excess (as may be determined by methods standard in the art) of at least 80% (i.e. at least 90% of one enantiomer and at most 10% of the other enantiomer), preferably at least 90% and more preferably at least 98%.
As used herein and unless otherwise stated, the term " solvate " includes any combination which may be formed by a derivative of this invention with a suitable inorganic solvent (e.g. hydrates) or organic solvent, such as but not limited to alcohols, ketones, esters and the like.
Detailed description of the invention
In a first aspect, the present invention relates to a family of compounds represented by the structural formula (I):
wherein:
- Ri is an acyl or sulfonyl group, in particular Ri is -C(=O)-R4 or -S(=O)2-R4,
- R4 is selected from the group consisting of R5, -OR5, -NHR5 and -SR5,
- R5 is selected from the group consisting of hydrogen; straight chain or branched chain, aliphatic or cycloaliphatic or aromatic groups such as C2-10 alkyl, 02-10 alkenyl, C2-io cycloalkyl, C2-10 alkynyl, aryl, arylalkyl, and saturated, partly unsaturated or aromatic heterocyclic groups,
- R2 is an acyl group selected from the group consisting of acyl groups derived from cycloaliphatic, aromatic or heterocyclic monocarboxylic acids, imidazolylcarbonyl or triazolylcarbonyl, in particular R2 is -C(=O)-R6,
- R6 is selected from the group consisting of aliphatic or cycloaliphatic or aromatic groups such as C2-10 alkyl, 03.10 cycloalkyl, C2-io alkenyl, C2-io alkynyl, aryl, arylalkyl and saturated, partly unsaturated or aromatic heterocycleic groups, - R3 is hydrogen or an amino-protecting group, in particular R3 is hydrogen, -C(=O)-R7, -C(=O)-OR7 or aryl-Ci-7alkyl; and
- R7 is C1-10 alkyl, C2-io alkenyl, aryl, or aryl-Ci-i0 alkyl, wherein each of said alkyl, alkenyl or aryl may be substituted with one or more substituents independently selected from the group consisting of halogen, alkyl, alkoxy, nitro, cyano and hydroxy, As well as stereoisomers thereof, solvates thereof, or salts thereof.
Within this broad acceptance of the invention, each generic term such as, but not limited to, " acyl ", " sulfonyl ", " heterocyclic " , " cycloaliphatic " and " aromatic " may, independently from each other, be understood according to any of the particular meanings thereof indicated in the above definitions.
A first embodiment of this aspect of the invention relates to compounds wherein Ri is an acyl group derived from an aliphatic, cycloaliphatic, aromatic or heterocyclic monocarboxylic acid. Ri may be different from R2, especially when Ri is an aliphatic acyl group. Alternatively, according to a second embodiment of this aspect of the invention, when Ri is an acyl group derived from a cycloaliphatic, aromatic or heterocyclic monocarboxylic acid, Ri may be the same as R2.
In view of the commercial availability of the starting materials, a preferred embodiment of this aspect of the invention relates to compounds wherein Ri is selected from the group consisting of benzoyl, p-toluoyl, 1- naphthalenecarbonyl, 2-naphthalenecarbonyl, 4-morpholinocarbonyl, 1-piperi- dinocarbonyl, 1-imidazolidinocarbonyl, 1-pyrrolidinocarbonyl, 2-thiazole- carbonyl, 1-methyl-1 H-pyrrole-2-carbonyl, 2-furanecarbonyl, 3-furanecarbonyl, 3-pyridinecarbonyl, 4-pyridinecarbonyl, 2-thiophenecarbonyl, cyclobutane- carbonyl, cyclopentanecarbonyl, cyclohexanecarbonyl, 1-adamantane- carbonyl, pipecolinyl and 2-norbornanecarbonyl. Another embodiment of this aspect of the invention relates to compounds wherein Ri is selected from the group consisting of acetyl, formyl, propanoyl, butanoyl and pentanoyl.
Another embodiment of this aspect of the invention relates to compounds wherein R3 is the same as R2. Suitable amino-protecting groups such as required for R3 are well known in the art and are preferably selected from the group consisting of arylcarbonyl, alkyloxycarbonyl and arylalkyloxycarbonyl. A few non-limiting examples of suitable amino-protecting groups include benzyloxycarbonyl (which may be introduced by reaction with benzylchloroformate under alkaline conditions, e.g. making use of sodium hydroxide or hydrogenocarbonate) and 9-fluorenylmethoxycarbonyl (which may be introduced by reaction with 9- fluorenylmethyl chloroformate). Another example of an amino-protecting group is a ferf-butoxycarbonyl group which may be introduced by reaction with di- tert-butyl dicarbonate under alcaline conditions. Other suitable amino- protecting groups for R3 include, but are not limited to aralkyl type protecting groups comprising benzyl, p-methoxybenzyl, p-nitrobenzyl, p-bromobenzyl and triphenylmethyl (trityl); alternative acyl type protecting groups comprising formyl, acetyl, chloroacetyl, dichloroacetyl, trichloroacetyl, trifluoroacetyl, phenylacetyl, o-nitrophenoxyacetyl, sec-butyryl, pivaloyl- (also known as tert- butyryl), cyclopropanoyl, benzoyl, o-nitrobenzoyl, and alpha-chlorobutyryl; or other urethane type protecting groups comprisingbenzyloxycarbonyl, p- chlorobenzyloxycarbonyl, p-nitrobenzyloxycarbonyl, p-bromobenzyloxy- carbonyl, p-methoxybenzyloxycarbonyl, o-nitrobenzyloxycarbonyl, tert- butyloxycarbonyl, te/t-amyloxycarbonyl, diisopropylmethoxycarbonyl, isopropyloxycarbonyl, allyloxycarbonyl, cyclopentyloxycarbonyl, adamantyl- oxycarbonyl and cyclohexyloxycarbonyl.
Still another embodiment of the present invention relates to compounds represented by the structural formula (I), wherein when R4 is R5 and Ri is - C(=O)-R4 then a heterocyclic group R5 (i.e. R4) may be attached through one of its heteroatoms to the carbon atom of the carbonyl group of Ri.
Still another embodiment of the present invention relates to compounds represented by the structural formula (I), wherein a heterocyclic group Re may be attached through one of its heteroatoms to the carbon atom of the carbonyl group of R2.
For pharmaceutical use, especially for the formulation of suitably bioavailable drug formulations, it may be particularly preferred that the compound of the invention is present in the form of a non-toxic acid addition salt, more preferably a pharmaceutically acceptable acid addition salt, of a compound defined according to the above structural formula and wherein R3 is hydrogen. The latter form includes any therapeutically active non-toxic addition salt which the compounds of this invention are able to form with a (preferably pharmaceutically acceptable) salt-forming agent. Such addition salts may conveniently be obtained by treating the compounds of the invention with an effective amount (preferably an at least stoechiometric amount) of an appropriate salt-forming acid, while using reaction conditions (such as, but not limited to, temperature, pressure, time and the like) conventional in the art for such treatment. For instance, compounds having basic properties such as the amino compounds of the present invention, may conveniently be converted into the corresponding therapeutically active, non-toxic acid addition salt form by treating the free base form with a suitable amount of an appropriate acid following conventional procedures. Examples of such appropriate salt-forming acids include, for instance, inorganic acids resulting in forming salts such as, but not limited to, hydrohalides (e.g. hydrochloride and hydrobromide), sulfate, nitrate, phosphate, diphosphate, carbonate, bicarbonate, and the like; and organic monocarboxylic or dicarboxylic acids resulting in forming salts such as, but not limited to, acetate, propanoate, hydroxyacetate, 2- hydroxypropanoate, 2-oxopropanoate, lactate, pyruvate, oxalate, malonate, succinate, maleate, fumarate, malate, tartrate, citrate, methanesulfonate, ethanesulfonate, benzoate, 2-hydroxybenzoate, 4-amino-2-hydroxybenzoate, benzene-sulfonate, p-toluenesulfonate, salicylate, p-aminosalicylate, pamoate, bitartrate, camphorsulfonate, edetate, 1 ,2-ethanedisulfonate, fumarate, glucoheptonate, gluconate, glutamate, hexylresorcinate, hydroxynaphtoate, hydroxyethanesulfonate, mandelate, methylsulfate, pantothenate, stearate, as well as salts derived from ethanedioic, propanedioic, butanedioic (Z)-2- butenedioic, (E)2-butenedioic, 2-hydroxybutanedioic, 2,3-dihydroxybutane- dioic, 2-hydroxy-1 ,2,3-propanetricarboxylic, cyclohexanesulfamic acids and the like.
An advantage of the present invention is that compounds defined according to the above structural formula are easily accessible in good yield and purity through a synthetic scheme involving a limited number of process steps and starting from commercially available materials. An exemplary but non-limiting method for preparing the compounds of this invention comprises the steps of:
(a) reacting synephrine with an amino-protecting reagent to form an amino- protected synephrine, (b) reacting said amino-protected synephrine with a chloride selected from the group consisting of carboxylic acid chlorides, carbamic acid chlorides, chloroformates, thiocarboxylic acid chlorides, imidic acid chlorides and sulfonic acid chlorides to produce a 4-[2-(N-protected-methylamino)-1- hydroxyethyl] phenyl ester, in particular 4-[2-(N-protected-methylamino)-1- hydroxyethyl] phenyl benzoate, and
(c) reacting said 4-[2-(N-protected-methylamino)-1-hydroxyethyl]phenyl ester, in particular said 4-[2-(N-protected-methylamino)-1-hydroxyethyl]phenyl benzoate, with an activated carbonyl compound selected from the group consisting of carboxylic acid chlorides, carbamic acid chlorides, chloroformates, thiocarboxylic acid chlorides, imidic acid chlorides, 1 ,1'- carbonyldiimidazole and 1 ,1 '-carbonylditriazole.
Carboxylic acid chlorides suitable for use in the synthesis of the compounds of the present invention include benzoyl chlorides such as, but not limited to, benzoyl chloride, p-anisoyl-chloride, 2-bromobenzoyl chloride, 4- bromobenzoyl chloride, 3-chlorobenzoyl chloride, pentafluorobenzoyl chloride, 2-chlorobenzoyl chloride, p-toluoyl chloride, 4-chlorobenzoyl chloride, 2,4- dichlorobenzoyl chloride, 3,4-dichlorobenzoyl chloride, 4-nitrobenzoyl chloride, 4-fluorobenzoyl chloride, 2-fluoro-benzoyl chloride, o-toluoyl chloride, m- toluoyl chloride, 4-cya no benzoyl chloride, 3-nitrobenzoyl chloride, 4-tert-butyl- benzoyl chloride, 4-biphenylcarbonyl chloride, 3,5-dimethoxybenzoyl chloride, 3-fluorobenzoyl chloride, 2,6-dichlorobenzoyl chloride, 4-butylbenzoyl chloride, 4-heptyloxybenzoyl chloride, 4-hexylbenzoyl chloride, 4-hexyloxybenzoyl chloride, 4-pentylbenzoyl chloride, m-anisoyl chloride, 2,6-difluoro-benzoyl chloride, 2-nitrobenzoyl chloride, 4-chloro-3-nitrobenzoylchloride, 3,4-difluoro- benzoyl chloride, 2-iodobenzoyl chloride, 1-naphthoyl chloride, o-anisoyl chloride, 2,4-difluorobenzoyl chloride, 4-(trifluoromethyl)benzoyl chloride, m- anisoyl chloride, 2,6-difluorobenzoyl chloride, 2-nitrobenzoyl chloride, 4- chloro-3-nitro-benzoylchloride, 3,4-difluorobenzoyl chloride, 2-iodobenzoyl chloride, 1-naphthoyl chloride, o-anisoyl chloride, 2,4-difluorobenzoyl chloride, 4-(trifluoromethyl)benzoyl chloride, 3-(chloro-methyl)-benzoyl chloride, A- (chloromethyl)-benzoyl chloride, 3-(dichloromethyl)-benzoyl chloride, 2,3,4,5- tetrafluorobenzoyl chloride, 2,4,6-trichlorobenzoyl chloride, 2,3,4- trifluorobenzoyl chloride, 2,4,6-trifluorobenzoyl chloride, 4-bromo-2-fluoro- benzoyl chloride, 2,3,5,6-tetrafluorobenzoyl chloride, 3,5-dinitrobenzoyl chloride, 4-heptylbenzoyl chloride, 4-iodobenzoyl chloride, 4-octylbenzoyl chloride, 4-pentyl-oxybenzoyl chloride, 4-phenylazobenzoyl chloride, A- propylbenzoyl chloride, methyl 4-chloro-carbonylbenzoate, 3,5- dichlorobenzoyl chloride, 3-fluoro-4-trifluoromethyl-benzoyl chloride, 2,6- dimethoxybenzoyl chloride, piperonyloyl chloride, 2,4-dimethoxybenzoyl chloride, 3,4-dihydro-2H-1 ,5-benzodioxepine-6-carbonyl chloride, 2,3-dihydro- 1 ,4-benzodioxine-6-carbonyl chloride, 2,3-dihydro-1 ,4-benzodioxine-5- carbonyl chloride, 1-benzofuran-5-carbonyl chloride, 2,1 ,3-benzothiadiazole-4- carbonyl chloride, 2,1 ,3-benzothiadiazole-5-carbonyl chloride, 1 ,2,3- benzothia-diazole-5-carbonyl chloride, 2,1 ,3-benzoxadiazole-5-carbonyl chloride, 6-quinoxaline-carbonyl chloride, 4-(2-thienyl)-benzoyl chloride, A- methyl-3,4-dihydro-2H-1 ,4-benzoxazine-7-carbonyl chloride, 4-(1 ,2,3- thiadiazol-4-yl)benzoyl chloride, 4-(1 H-pyrazol-1-yl)benzoyl chloride, 1-methyl- 1 H-1 ,2,3-benzotriazole-5-carbonyl chloride, i-benzothiophene-5-carbonyl chloride, 2,2-dimethyl-2,3-dihydro-1-benzofuran-7-carbonyl chloride, A- [(dipropyl-amino)sulfonyl] benzene-1 -carbonyl chloride, 4-[3-(trifluoromethyl)- 1 H-pyrazol-1-yl]-benzoyl chloride, 2-bromo-5-methoxybenzene-1 -carbonyl chloride, 5-bromo-2,3,4-trimethylbenzoyl chloride, 2-chloro-6-fluorobenzene-1- carbonyl chloride, 2, 3-dimethylbenzene-1 -carbonyl chloride, 3,4- dimethylbenzene-1 -carbonyl chloride, 2-chloro-4-fluorobenzoyl chloride, 5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthalene-carbonyl chloride, 2-(4- methoxyphenoxy)-5-nitrobenzene-1 -carbonyl chloride, 2,3-difluorobenzoyl chloride, 2-fluoro-5-(trifluoromethyl)benzoyl chloride, 2,3,6-trifluoro-benzoyl chloride, 1-isopropyl-1 H-1 ,2,3-benzotriazole-5-carbonyl chloride, 1-isopropyl- 1 H-1 ,2,3-benzotriazole-5-carbonyl chloride, 3-fluoro-4-methylbenzoyl chloride, 3-(cyclo-pentyloxy)-4-methoxybenzoyl chloride, 4-fluoro-3-
(trifluoromethyl)benzoyl chloride, 2,3-dihydro-i -benzofuran-7-carbonyl chloride, 3-(2-methyl-thiazol-4-yl)-benzoyl chloride, 1-isopropyl-2- (trifluoromethyl)-i H-benzimida-zole-5-carbonyl chloride, 5-bromo-2,3-di- hydrobenzo[b]furan-7-carbonyl chloride, 2,4,6-trimethylbenzoyl chloride, 2-(2- thienyl)-benzoyl chloride, 3-cyanobenzoyl chloride, acetylsalicyloyl chloride, 3- (5-methyl-1 ,2,4-oxadiazol-3-yl)-benzoyl chloride, and 4-(5-methyl-1 ,2,4- oxadiazol-3-yl)-benzoyl chloride.
Numerous other carboxylic acid chlorides are known to the person skilled in the art and commercially available for use as acylating reagent for use in the above reaction step. Particular carbonyl chlorides for use in the method of the invention include, but are not limited to, cinnamoyl chloride, hydrocinnamoyl chloride, 2-phenylbutyryl chloride, phenylacetyl chloride and 4-fluorophenylacetyl chloride.
Phenylsulfonyl chlorides (represented by the structural formula V-B) suitable for use in the synthesis of the compounds of the present invention include, but are not limited to, 4-fluorobenzenesulfonyl chloride, 2- mesitylenesulfonyl chloride, 4-methoxybenzene-sulfonyl chloride, p- toluenesulfonyl chloride, pentafluorobenzene-sulfonyl chloride, benzenesulfonyl chloride, 4-bromobenzenesulfonyl chloride, N-acetylsulfanilyl chloride, 2,4,6-triisopropyl-benzenesulfonyl chloride 2- naphthalenesulfonylchloride, 4-chloro-benzenesulfonyl chloride 3,5-dichloro-2- hydroxy-benzenesulfonylchloride, 2,5-dichloro-benzenesulfonyl chloride, pipsyl chloride, 1 -naphthalenesulfonylchloride, methyl 2-(chlorosulfonyl)- benzoate, 4-tert-butylbenzene-sulfonyl chloride, 3-(trifluoromethyl) benzenesulfonyl chloride, 2-bromobenzenesulfonyl chloride, 4-acetylbenzene- sulfonylchloride, 2-(trifluoromethyl)-benzenesulfonyl chloride, 3,4- dichlorobenzene-sulfonyl chloride, 3,4-dimethoxybenzenesulfonyl chloride, 3- chlorobenzenesulfonyl chloride, 2-chloro-4-fluorobenzenesulfonyl chloride, 3,5-dichlorobenzenesulfonyl chloride, 3-chloro-4-fluorobenzenesulfonyl chloride, 2,4-dichlorobenzenesulfonyl chloride, 2,5-dimethoxybenzenesulfonyl chloride, 3-bromo-benzenesulfonyl chloride, 2,3-dichlorobenzenesulfonyl chloride, 5-fluoro-2-methylbenzenesulfonyl chloride, 3-fluorobenzenesulfonyl chloride, 2,3,5,6-tetramethyl-benzenesulfonyl chloride, 3-chloro-2- methylbenzenesulfonyl chloride, 2,5-dibromo-3,6-difluoro-benzenesulfonyl chloride, 2,6-difluorobenzenesulfonyl chloride, 2-chloro-benzenesulfonyl chloride, 5-bromo-2-methoxybenzenesulfonyl chloride, 5-chloro-2- methoxybenzenesulfonyl chloride, 2,4-difluorobenzenesulfonyl chloride, 2- cyano-benzenesulfonyl chloride, 2-chloro-5-(trifluoromethyl)-benzenesulfonyl chloride, 4-bromomethylbenzenesulfonyl chloride, 2,4- dimethoxybenzenesulfonyl chloride, 4-chloro-3-nitrobenzenesulfonyl chloride, 4-(chlorosulfonyl)-benzoic acid, 3-nitro-benzenesulfonyl chloride, 4- nitrobenzenesulfonyl chloride, 2-(methylsulfonyl)-benzenesulfonyl chloride, 4- (methylsulfonyl)-benzene-sulfonyl chloride, 3-(chloro-sulfonyl)-benzoic acid, 2,4-dichloro-5-methylbenzene-sulfonyl chloride, 4-(trifluoro-methoxy)- benzenesulfonyl chloride, 2-methoxy-4-nitrobenzenesulfonyl chloride, 4- bromo-2-chlorobenzenesulfonyl chloride, 2,3-dihydro-1 -benzofuran-5-sulfonyl chloride, 2,3-dihydro-1 ,4-benzodioxine-6-sulfonyl chloride, 1 ,3-benzothiazole- 6-sulfonyl chloride, 2,1 ,3-benzothiadiazole4sulfonyl chloride, 2,1 ,3- benzothiadiazole-5-sulfonyl chloride, 2,1 ,3-benzoxadiazole-4-sulfonyl chloride, 3,4-dihydro-2H-1 ,5-benzodioxepine-7-sulfonyl chloride, 4-methyl-3,4-dihydro- 2H-1 ,4-benzoxazine-7-sulfonyl chloride, 4-(1 ,3-oxazol-5-yl)benzenesulfonyl chloride, 4-(1 ,2,3-thiadiazol-4-yl)benzenesulfonyl chloride, 4-(1 H-pyrazol-1- yl)benzenesulfonyl chloride, 4-(3-chloro-2-cyanophenoxy)benzene-1 -sulfonyl chloride, δ-chlorosulfonyl^-hydroxy-benzoic acid, 4-bromo-2,5-difluoro- benzene-1 -sulfonyl chloride, 4-(acetylamino)-3-chloro-benzene-1 -sulfonyl chloride, 3,5-di-(trifluoromethyl)-benzene-1 -sulfonyl chloride, 2- fluorobenzenesulfonyl chloride, 4-methyl-3-nitrobenzene-1 -sulfonyl chloride, 5-chloro-2,1 ,3-benzoxadiazole-4-sulfonyl chloride, 3-(5-methyl-1 ,3,4- oxadiazol-2-yl) benzenesulfonyl chloride, methyl 3-(chlorosulfonyl)-4- methoxybenzoate, 4-bromo-2-(trifluoromethyl)-benzenesulfonyl chloride, 2,2- dimethyl-6-chromanesulfonyl chloride, 4-(morpholine-4-sulfonyl) benzenesulfonyl chloride, 4-(pyrrolidine-1-sulfonyl)-benzene-sulfonyl chloride, 3-(2-methyl-4-pyrimidinyl)benzenesulfonyl chloride, 2-cyano-5- methylbenzenesulfonyl chloride, 2,5-dimethylbenzenesulfonyl chloride, 4- chloro-3-(trifluoromethyl)-benzene-sulfonyl chloride, 4-bromo-2- methylbenzene-1 -sulfonyl chloride, 2-chloro-4-(trifluoro-methyl)-benzene-1 - sulfonyl chloride, 2-chloro-4-cyano-benzene-1 -sulfonyl chloride, 2,6-dichloro- 4-(trifluoromethyl)-benzene-1 -sulfonyl chloride, 3,4-difluorobenzene-1 -sulfonyl chloride, 2-iodobenzene-1 -sulfonyl chloride, 4-methyl-1-naphthalenesulfonyl chloride, 4-(trifluoromethyl)benzene-1 -sulfonyl chloride, 2,6-dichlorobenzene- 1 -sulfonyl chloride, 2-(trifluoromethoxy)benzene-1 -sulfonyl chloride, 4- cyanobenzene-1 -sulfonyl chloride, 4-butoxybenzene-1 -sulfonyl chloride, 2,3,4- trifluorobenzene-1 -sulfonyl chloride, 4-bromo-2-(trifluoromethoxy) benzene-1- sulfonyl chloride, 3-cyanobenzene-1 -sulfonyl chloride, 3-chloro-4- methylbenzene-1 -sulfonyl chloride, 4-bromo-2-ethyl-benzene-1 -sulfonyl chloride, 5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthalene-sulfonyl chloride, 4-(2-chloro-6-nitrophenoxy)benzene-1 -sulfonyl chloride, 3,5-dichloro- 4-(2-chloro-4-nitrophenoxy) benzene-1 -sulfonyl chloride, 4-pentylbenzene-1- sulfonyl chloride, 4-ethylbenzene-1 -sulfonyl chloride, 4-propylbenzene-1- sulfonyl chloride, 4-butylbenzene-1 -sulfonyl chloride, 3-toluenesulfonyl chloride, 4-isopropyl-benzenesulfonyl chloride, 4-(2-oxo-1- pyrrolidinyl)benzene sulfonyl chloride, 4-(2-methoxyphenoxy)benzenesulfonyl chloride, 4-(2-chloro-phenoxy)benzenesulfonyl chloride, 4-(2-methylphenoxy) benzenesulfonyl chloride, 4'-chloro(1 ,1'-biphenyl)-4-sulfonyl chloride, 4'- fluoro(1 ,1'-biphenyl)-4-sulfonyl chloride, 4'-methoxy-(1 ,1 '-biphenyl)-4-sulfonyl chloride, 3\4'-dichloro-(1 ,1'-biphenyl)-4-sulfonyl chloride, 4- phenoxybenzenesulfonyl chloride, 4'-methyl-(1 ,1'-biphenyl)-4-sulfonyl chloride, 5-bromo-2,3-dihydrobenzo[b]furan-7-sulphonyl chloride, 3,4,5-trifluoro- benzenesulfonyl chloride, 3-(5-methyl-1 ,2,4-oxadiazol-3-yl)benzenesulfonyl chloride, 4-(2-methyl-1 ,3-thiazol-4-yl)benzenesulfonyl chloride, 1-acetyl-5- indolinesulfonyl chloride, 3-(2-methyl-1 ,3-thiazol-4-yl)benzene-sulfonyl chloride and 1 ,3-benzodioxole-5-sulfonyl chloride.
Phenylacetyl chlorides also suitable for use in the synthesis of the compounds of the present invention include, but are not limited to, phenylacetyl chloride, 4-methoxyphenylacetyl chloride, 2-(2-naphthyl)acetyl chloride, 2-(3,5-difluorophenyl)ethanoyl chloride, 2-(1-naphthyl)ethanoyl chloride, 4-chlorophenylacetyl chloride, 3-methoxyphenylacetyl chloride, and 4-fluorophenylacetyl chloride.
The above method is able to provide compounds defined according to the above structural formula and wherein R3 is an amino-protecting group such as referred herein above or, in the presence of an additional final step, wherein R3 is hydrogen .
Suitable experimental conditions for performing protection step (a) are well known in the art. An exemplary but non-limiting embodiment of the method of the invention includes a step (a) comprising reacting synephrine with an amino-protected thiazolidine-2-thione. Preferably, the amino-protected thiazolidine-2-thione or other amino-protecting reagent may be dissolved in an organic solvent such as an ether for use in said step (a), and is preferably used in a molar ratio of at least 1 :1 , more preferably from 1 :1 to about 2:1 , with respect to synephrine. Preferably the reaction of step (a) is performed in a solvent system which may comprise water, a lower alcohol (such as, but not limited to, methanol), and optionally in the presence of a further organic solvent (such as the solvent used for introducing the amino-protected thiazolidine-2-thione or other amino-protecting reagent). When the amino-protected thiazolidine-2-thione used in step (a) is tert- butoxycarbonyl-thiazolidine-2-thione, step (a) results into a terf-butoxy- carbonyl-protected synephrine as an intermediate readily available, optionally without further purification, for the subsequent step (b).
In step (b), said N-protected synephrine is reacted with a suitable chloride for introducing the relevant substituent R-i. Suitable experimental conditions for performing acylation or sulfonation step (b), especially the molar ratio between the selected acylating or sulfonating agent and the N-protected synephrine are well known in the art and, depending upon the selected acylating or sulfonating agent, and the number of hydroxyl groups to be acylated or sulfonated, may be tailored at will without undue experimentation.
In step (c), said N-protected and acylated or sulfonated synephrine is reacted with a suitable activated carbonyl compound for introducing the relevant substituent R2. Suitable experimental conditions for performing said step (c) are well known in the art and, depending upon the selected activated carbonyl compound, may be tailored at will without undue experimentation. It should be realized, however, that when R2 is imidazolylcarbonyl or triazolylcarbonyl, a limited number of activated carbonyl compounds are available for efficiently introducing the substituent R2. In the latter situation, the activated carbonyl compound should preferably be carbonyldiimidazole or, respectively, carbonylditriazole, both being well known for their selective activation capacity.
When compounds defined according to the above structural formula and wherein R3 is hydrogen are desired, the above-referred general synthetic method preferably further comprises a step (d) for selectively deprotecting the amino group of the compound resulting from step (c), without affecting any of groups Ri and R2 being present in said compound. For instance the amino- protecting group may be removed by deprotection methods conventional in the art, such as:
- when the amino-protecting group is a phenylmethoxycarbonyl group, cleavage of the benzylic ether function by hydrogenolysis, e.g. using H2, Pd-C at about 25°C, or under strongly acidic conditions (e.g. making use of bromhydric acid), or - when the amino-protecting group is a tert-butoxycarbonyl group, by treatment with an acid, e.g. using aqueous hydrochloric acid or trifluoroacetic acid, under conditions mild enough to avoid further cleavage of the molecule, or
- when the amino-protecting group is a 9-fluorenylmethoxycarbonyl group, by treatment with a base such as piperidine.
As is well known in the art, the method of said step (d) may be capable of simultaneously achieving selective deprotection of the amino group and the formation of a non-toxic acid addition salt such as, but not limited to, a hydrochloride, a hydrobromide or a trifluoroacetate, of the compounds of the invention wherein R3 is hydrogen. This particular aspect of the invention may be useful when the said compound is intended for formulation into a medicament since the water-solubility of the said salt is expected to be significantly higher than that of the corresponding free base form of said compound. In another aspect, based on the fact that the above-defined novel synephrine derivatives exhibit biologically-active properties, the present invention relates to a pharmaceutical composition comprising a therapeutic effective amount of a compound defined by the above structural formula (with any of the available individual meanings for each of R1, R2 and R3), and optionally one or more pharmaceutically acceptable carriers or excipients. Said pharmaceutical composition may comprise a novel synephrine derivative of the invention as the single bio-active ingredient, or as a bio-active ingredient in combination with one or more other drugs in a combined preparation for a so-called combination therapy.
The term " pharmaceutically acceptable carrier or excipient " as used herein in relation to pharmaceutical compositions and combined preparations means any material or substance with which the bio-active principle(s), i.e. the synephrine derivative and the said one or more other drugs, may be formulated in order to facilitate application or dissemination to the locus to be treated, for instance by dissolving, dispersing or diffusing the said composition, and/or to facilitate its storage, transport or handling without impairing its effectiveness. The pharmaceutically acceptable carrier may be a solid or a liquid or a gas which has been compressed to form a liquid, i.e. the compositions of this invention can suitably be used in the form of concentrates, emulsions, solutions, granulates, dusts, sprays, aerosols, pellets or powders, but are not limited thereto.
Suitable pharmaceutical carriers or excipients for use in the said pharmaceutical compositions and their formulation are well known to those skilled in the art. There is no particular restriction to their selection within the present invention although, in case of a low or very low water-solubility of the synephrine derivative of this invention, special attention must be paid to the selection of suitable carrier combinations that can assist in a proper formulation in view of the expected time release profile. Suitable pharmaceutical carriers or excipients include additives such as, but not limited to, wetting agents, dispersing agents, stickers, adhesives, emulsifying or surface-active agents, thickening agents, complexing agents, gelling agents, solvents, coatings, antibacterial and antifungal agents (for example phenol, sorbic acid, chlorobutanol), isotonic agents (such as sugars or sodium chloride) and the like, provided that the same are consistent with standard pharmaceutical practice, i.e. carriers and additives which do not create severe and/or permanent damage to the mammal, in particular the human being, to be treated with said medicament. The pharmaceutical compositions of the present invention may be prepared by any method well known in the art, for instance by homogeneously mixing, dissolving, spray-drying, coating and/or grinding the bio-active ingredient(s), in a one-step or a multi-steps procedure, with the selected carrier material(s) and, where appropriate, the other additives such as surface-active agents. The pharmaceutical compositions of the present invention may also be prepared by micronisation, for instance in view to obtain them in the form of microspheres usually having a diameter of about 1 to about 10 μm, namely for the manufacture of microcapsules for controlled or sustained release of the said biologically-active ingredient(s).
Suitable surface-active agents useful as a pharmaceutically acceptable carrier or excipient in the pharmaceutical compositions of the present invention include non-ionic, cationic and/or anionic surfactants having good emulsifying, dispersing and/or wetting properties. Suitable anionic surfactants include both water-soluble soaps and water-soluble synthetic surface-active agents. Suitable soaps are alkaline or alkaline-earth metal salts, non- substituted or substituted ammonium salts of higher fatty acids (C10-C22). e.g. the sodium or potassium salts of oleic or stearic acid, or of natural fatty acid mixtures obtainable form coconut oil or tallow oil. Synthetic surfactants include sodium or calcium salts of polyacrylic acids; fatty sulphonates and sulphates; sulphonated benzimidazole derivatives and alkylarylsulphonates. Fatty sulphonates or sulphates are usually in the form of alkaline or alkaline-earth metal salts, non-substituted ammonium salts or ammonium salts substituted with an alkyl or acyl radical having from 8 to 22 carbon atoms, e.g. the sodium or calcium salt of lignosulphonic acid or dodecylsulphonic acid or a mixture of fatty alcohol sulphates obtained from natural fatty acids, alkaline or alkaline- earth metal salts of sulphuric or sulphonic acid esters (such as sodium lauryl sulphate) and sulphonic acids of fatty alcohol/ethylene oxide adducts. Suitable sulphonated benzimidazole derivatives preferably contain 8 to 22 carbon atoms. Examples of alkylarylsulphonates are the sodium, calcium or alcanolamine salts of dodecylbenzene sulphonic acid or dibutyl- naphtalenesulphonic acid or a naphtalene-sulphonic acid/formaldehyde condensation product. Also suitable are the corresponding phosphates, e.g. salts of phosphoric acid ester and an adduct of p-nonylphenol with ethylene and/or propylene oxide, or phospholipids. Suitable phospholipids for this purpose are the natural (originating from animal or plant cells) or synthetic phospholipids of the cephalin or lecithin type such as e.g. phosphatidylethanolamine, phosphatidylserine, phosphatidylglycerine, lysolecithin, cardiolipin, dioctanylphosphatidylcholine, dipalmitoylphoshatidyl- choline and their mixtures.
Suitable non-ionic surfactants useful as pharmaceutically acceptable carriers or excipients in the pharmaceutical compositions of the present invention include polyethoxylated and polypropoxylated derivatives of alkylphenols, fatty alcohols, fatty acids, aliphatic amines or amides containing at least 12 carbon atoms in the molecule, alkylarenesulphonates and dialkylsulphosuccinates, such as polyglycol ether derivatives of aliphatic and cycloaliphatic alcohols, saturated and unsaturated fatty acids and alkylphenols, said derivatives preferably containing 3 to 10 glycol ether groups and 8 to 20 carbon atoms in the (aliphatic) hydrocarbon moiety and 6 to 18 carbon atoms in the alkyl moiety of the alkylphenol. Further suitable non-ionic surfactants are water-soluble adducts of polyethylene oxide with poylypropylene glycol, ethylenediaminopolypropylene glycol containing 1 to 10 carbon atoms in the alkyl chain, which adducts contain 20 to 250 ethyleneglycol ether groups and/or 10 to 100 propyleneglycol ether groups. Such compounds usually contain from 1 to 5 ethyleneglycol units per propyleneglycol unit. Representative examples of non-ionic surfactants are nonylphenol-polyethoxyethanol, castor oil polyglycolic ethers, polypropylene/ polyethylene oxide adducts, tributylphenoxypolyethoxyethanol, polyethyleneglycol and octylphenoxypolyethoxyethanol. Fatty acid esters of polyethylene sorbitan (such as polyoxyethylene sorbitan trioleate), glycerol, sorbitan, sucrose and pentaerythritol are also suitable non-ionic surfactants.
Suitable cationic surfactants useful as pharmaceutically acceptable carriers or excipients in the pharmaceutical compositions of the present invention include quaternary ammonium salts, preferably halides, having 4 hydrocarbon radicals optionally substituted with halo, phenyl, substituted phenyl or hydroxy; for instance quaternary ammonium salts containing as N- substituent at least one Cβ-C-22 alkyl radical (e.g. cetyl, lauryl, palmityl, myristyl, oleyl and the like) and, as further sub-stituents, unsubstituted or halogenated lower alkyl, benzyl and/or hydroxy-lower alkyl radicals.
A more detailed description of surface-active agents suitable for this purpose may be found for instance in " McCutcheon's Detergents and
Emulsifiers Annual " (MC Publishing Crop., Ridgewood, New Jersey, 1981 ), "
Tensid-Taschenbuch ", 2nd ed. (Hanser Verlag, Vienna, 1981 ) and
"Encyclopaedia of Surfactants (Chemical Publishing Co., New York, 1981 ).
Structure-forming, thickening or gel-forming agents may be included into the pharmaceutical compositions and combined preparations of the invention. Suitable such agents are in particular highly dispersed silicic acid, such as the product commercially available under the trade name Aerosil; bentonites; tetraalkyl ammonium salts of montmorillonites (e.g., products commercially available under the trade name Bentone), wherein each of the alkyl groups may contain from 1 to 20 carbon atoms; cetostearyl alcohol and modified castor oil products (e.g. the product commercially available under the trade name Antisettle).
Gelling agents which may be included into the pharmaceutical compositions and combined preparations of the present invention include, but are not limited to, cellulose derivatives such as carboxymethylcellulose, cellulose acetate and the like; natural gums such as arabic gum, xanthum gum, tragacanth gum, guar gum and the like; gelatin; silicon dioxide; synthetic polymers such as carbomers, and mixtures thereof. Gelatin and modified celluloses represent a preferred class of gelling agents. Other optional excipients which may be included in the pharmaceutical compositions and combined preparations of the present invention include additives such as magnesium oxide; azo dyes; organic and inorganic pigments such as titanium dioxide; UV-absorbers; stabilisers; odor masking agents; viscosity enhancers; antioxidants such as, for example, ascorbyl palmitate, sodium bisulfite, sodium metabisulfite and the like, and mixtures thereof; preservatives such as, for example, potassium sorbate, sodium benzoate, sorbic acid, propyl gallate, benzylalcohol, methyl paraben, propyl paraben and the like; sequestering agents such as ethylene-diamine tetraacetic acid; flavoring agents such as natural vanillin; buffers such as citric acid and acetic acid; extenders or bulking agents such as silicates, diatomaceous earth, magnesium oxide or aluminum oxide; densification agents such as magnesium salts; and mixtures thereof. Additional carriers or excipients may be included in order to control the duration of action of the biologically-active ingredient(s) in the compositions and combined preparations of the invention. Control release compositions may thus be achieved by selecting appropriate polymer carriers such as for example polyesters, polyamino-acids, polyvinylpyrrolidone, ethylene-vinyl acetate copolymers, methylcellulose, carboxymethylcellulose, protamine sulfate and the like. The rate of drug release and duration of action may also be controlled by incorporating the active ingredient into particles, e.g. microcapsules, of a polymeric substance such as hydrogels, polylactic acid, hydroxymethyl-cellulose, polymethyl methacrylate and the other above- described polymers. Such methods include colloid drug delivery systems like liposomes, microspheres, microemulsions, nanoparticles, nanocapsules and so on. Depending on the route of administration, the pharmaceutical composition or combined preparation of the invention may also require protective coatings. Pharmaceutical forms suitable for injectable use include sterile aqueous solutions or dispersions and sterile powders for the extemporaneous preparation thereof. Typical carriers or excipients for this purpose therefore include biocompatible aqueous buffers, ethanol, glycerol, propylene glycol, polyethylene glycol, complexing agents such as, but not limited to, cyclodextrins, maltodextrins and the like, and mixtures thereof.
In another embodiment, this invention provides combinations, preferably synergistic combinations, of one or more synephrine derivatives represented by the above structural formula with one or more biologically-active drugs being preferably selected from the group consisting of anti-inflammatory drugs. As is conventional in the art, the evaluation of a synergistic effect in a drug combination may be made by analyzing the quantification of the interactions between individual drugs, using the median effect principle described by Chou et al. in Adv. Enzyme Reg. (1984) 22:27. Briefly, this principle states that interactions (synergism, additivity, antagonism) between two drugs can be quantified using the combination index (hereinafter referred as Cl) defined by the following equation: a -E^L EDlc x " EDx la + ED/2 wherein EDx is the dose of the first or respectively second drug used alone (1a, 2a), or in combination with the second or respectively first drug (1c, 2c), which is needed to produce a given effect. The said first and second drug have synergistic or additive or antagonistic effects depending upon Cl < 1 , Cl = 1 , or Cl > 1 , respectively. As will be explained in more detail herein-below, this principle may be applied to a number of desirable effects such as, but not limited to, an activity against inflammation. For instance the present invention relates to a pharmaceutical composition or combined preparation having synergistic effects against inflammation.
In yet another embodiment, this invention provides the use of a synephrine derivative represented by the above structural formula (with any of the available individual meanings for each of R-i, R2 and R3) for the manufacture of a medicament for preventing or treating an inflammatory disease or disorder. The compounds of the present invention have anti-inflammatory, analgesic and antipyretic activities comparable with glucocorticoids, but without side effects thereof, and are therefore safely useful in methods of treating or preventing diseases or conditions in which NF-κB and/or its target genes such as but not limited to IL-6, IL-8 and E-selectin are implicated. Such diseases and conditions include, but are not limited to, those in which inflammation or tissue injury is involved such as osteoarthritis, rheumatoid arthritis, ankylosing spondilytis and the like, as well as other rheumatologic or pain indications. Other diseases in which inflammation is involved and for which the novel compounds of the present invention are therapeutically useful include, but are not limited to, asthma, psoriasis, septic shock and inflammatory bowel disease. Since NF-κB may also be involved in apoptosis, the compounds of the present invention are also useful to limit tissue and/or cell damage and for ischaemic disease, neural injury or myocardial infarction. The compounds of the invention are also useful in the treatment or prevention of Alzheimer's disease by delaying the onset or slowing the progression of said disease.
In view of the above methods of treatment or prevention, the aforementioned compounds of the invention (with any of the available individual meanings for each of R-i, R2 and R3) or pharmaceutical compositions (formulations) thereof may be administered by any conventional method including oral and parenteral (e. g. subcutaneous, intraperitoneal, intravascular or intramuscular) injection. The treatment may consist of a single dose or a plurality of doses of the bio-active ingredient over a predetermined period of time.
Thus, the present invention involves a method of treating a patient having inflammation or an inflammation-related disorder by the administration of a therapeutically effective amount of a novel synephrine compound of the present invention. The invention is therefore useful for, but not limited to, the treatment of inflammation in a patient, and for treatment of other inflammation- associated disorders such as pain, headache or fever. The compounds of the present invention are also useful to treat arthritis, including but not limited to rheumatoid arthritis, spondylarthritis, gouty arthritis, osteoarthritis, systemic lupus erythematosus, and juvenile arthritis. The compounds of the present invention are also useful in the treatment of asthma, bronchitis, menstrual cramps, tendinitis, bursitis, and skin-related conditions such as psoriasis, eczema, acne, burns and dermatitis. Moreover, the compounds of the present invention are useful for the treatment of gastrointestinal inflammatory conditions such as, but not limited to, inflammatory bowel disease, Crohn's disease, gastritis, irritable bowel syndrome and ulcerative colitis. The compounds of the present invention are also useful in the treatment or prevention of inflammatory effects of cancer, such as colorectal cancer, breast cancer, prostate cancer or leukemia. The compounds of the present invention are further useful in treating inflammation in diseases such as vascular diseases, migraine, headache, periarteritis nodosa, thyroiditis, plastic anemia, Hodgkin's disease, chroniclymphocytic leukemia, scleroderma, rheumatic fever, type I diabetes, myasthenia gravis, multiple sclerosis, sarcoidosis, nephrotic syndrome, Bechet's syndrome, polymyositis, gingivitis, myocardial ischemia and the like. In addition, the compounds of the present invention are useful in the treatment of inflammatory effects of ophthalmic diseases such as retinitis, retinopathy, conjunctivitis, uveitis, ocular photophobia, and acute injury to the eye tissue. The compounds of the present invention are also useful in the treatment of pulmonary inflammation, such as one associated with viral infection or cystic fibrosis. The compounds of the present invention are further useful for the treatment of certain central nervous system disorders such as, but not limited to, cortical dementia, Alzheimer's disease, and multiple sclerosis. The compounds of the present invention are also useful in the treatment of allergic rhinitis, respiratory distress syndrome, endotoxin shock syndrome, atherosclerosis and central nervous system damage resulting from stroke, ischemia or trauma. Besides being useful for human treatment, the compounds of the present invention are also useful for the treatment of higher mammals, including pets and cattle such as, but not limited to, horses, dogs, cats, sheep and pigs.
The term " therapeutically-effective " as used herein refers to an amount of the bio-active agent for use in anti-inflammation therapy which achieves improvement in inflammation severity, as may be determined by any practical or reproducible method. For oral administration, the pharmaceutical composition of this invention may be in the form of a dosage unit containing a predetermined amount of the bio-active ingredient. Examples of such dosage units are tablets or capsules.
The therapeutically active amount of compound that can be administered and the dosage regimen for treating an inflammatory disease condition with a compound and/or pharmaceutical composition of this invention depends on a variety of factors, including the age, weight, sex and medical condition of the patient, the severity of the disease, the route and frequency of administration, and the particular compound used, and thus may vary in accordance with said factors. The pharmaceutical composition may contain the bio-active ingredient of this invention in a range from about 0.1 to about 2000 mg, preferably about 0.5 to 500 mg and more preferably about 1 to 100 mg per dosage unit. A daily dose of about 0.01 to 100 mg/kg body weight, preferably about 0.1 to 20 mg/kg body weight and more preferably about 0.1 to 10 mg/kg body weight, may be appropriate for administration to a human being. The daily dose may suitably be administered in one to four sub-doses per day. In the case of psoriasis and other skin inflammatory conditions, it may be preferred to apply a topical preparation of the compound of this invention to the affected area two to four times per day.
The following examples are provided for illustration of the invention without limiting its scope in any way, and will be explained with reference to the general scheme 1 below.
R., = -alkyl, -aryl, -o-alkyl, -o-aryl R1=R2 = -alkyl, -aryl
Scheme 1
EXAMPLE 1 - preparation of a N-protected svnephrine The following refers to the preparation of N-protected synephrines according to scheme 1 , step a.
Synephrine (referred as 13 in the above scheme 1 ) (1.65 g, 9.87 mmol) was dissolved in a boiling mixture of water (25 ml) and methanol (12 ml). This hot solution was stirred vigorously, and then a yellow solution of a N-acyl thiazolidine-2-thione (referred to as 14 in the above scheme 1 ; for the purpose of the present example N-acetyl-thiazolidine-2-thione (14a) was used) (1.592 g, 9.87 mmol) in THF (10 ml) was added portion-wise. Disappearance of the yellow color was nearly instantaneous, however in order to ensure complete reaction, triethyl amine (202 mg, 2 mmol) was added, and after 10 minutes the resulting colorless solution was cooled to 400C and concentrated under reduced pressure onto a rotary evaporator. The crude product was purified by column chromatography using 200 g of silica gel and eluting with 300 ml of a 98:2 (volume ratio) CH2CI2-methanol mixture, followed by a 94:6 (volume ratio) CH2CI2-methanol mixture. The desired product (1.40 g, yield 72 %) may be re-crystallized from ethyl acetate.
EXAMPLE 2 - preparation of Λ/-Boc-synephrine: tert-butyl [2-hydroxy-2-(4- hydroxyphenvDethyllmethylcarbamate Synthesis of N-Boc Synephrine was carried out as described in example 1 but using Λ/-te/?-butyloxycarbonyl thiazolidine-2-thione (Λ/-Boc- thiazolidine-2-thione) as the N-acyl thiazolidine-2-thione. N-Boc-thiazolidine-2- thione may be easily obtained by reacting di-terf-butyl dicarbonate with 1 ,3- thiazolidine-2-thione preferably in the presence of an organic base such as triethylamine.
One molar equivalent of N-Boc thiazolidine-2-thione was added to a boiling solution of synephrine in methanol and water followed by one molar equivalent of triethyl amine. The solution was maintained at 7O0C. The crude resulting product was purified by column chromatography using a mixture of CH2CI2 and MeOH in a volume to volume ratio of 98:2, to yield 85% of the pure crystalline material.
EXAMPLE 3 - preparation of N-protected-di-O-acyl-svnephrines
The following refers to the preparation of N-protected-di-O-acyl- synephrines according to scheme 1 , step b.
Dry methylene chloride (17 ml) and triethylamine (346 mg, 3.42 mmol) were added to a 50 ml round bottom flask containing the N-protected synephrine obtained in example 1 (1.71 mmol). This mixture was stirred at room temperature until a slightly turbid solution was obtained. The flask was placed under nitrogen pressure and immersed into an ice bath. An acyl chloride (3.42 mmol) was then added drop-wise within four minutes to the chilled solution. The ice bath was removed two minutes after addition was completed, and the reaction solution was stirred at room temperature for 43 hours. The reaction flask was chilled in an ice bath, and addition of 0.25 equivalent of triethylamine followed by drop-wise addition of 0.25 equivalent of the same acyl chloride was carried out. After one hour, thin layer chromatography (TLC) analysis (performed with a 98:2 (volume ratio) ChbCVmethanol mixture indicated that reaction was complete. The reaction solution was diluted with methylene chloride and extracted with a half- saturated NaHCθ3 solution. The organic layer was dried over anhydrous MgSO4, filtered and concentrated into an oil. The crude material obtained was purified by column chromatography (100 g silica gel, 98:2 (volume ratio) CH2Cl2/methanol mixture) to afford the desired product with a yield of about 70%.
EXAMPLE 4 - preparation of 4-(2-r(ferf-butoxycarbonvD(methyl)arninol-1- hydroxyethyllphenyl benzoate and related derivatives
The following refers in general to the preparation of N-protected synephrine derivatives according to scheme 1 , step c.
To a N-protected synephrine, in particular for the purpose of the present example N-BOC synephrine as obtained in example 2 (1.75 mmole) dissolved in 6 ml methanol was added solid potassium hydroxide (85 mg, 1.516 mmole). The mixture was stirred until full KOH dissolution, then methanol was removed under reduced pressure. The resulting residue was dried under vacuum, placed under a nitrogen atmosphere and then stirred in 3 ml of dry DMF. Once dissolution was effected, an acyl chloride such as benzoyl chloride (1.516 mmole) was added drop-wise so that only slight warming was observed. TLC analysis with a 96:4 (volume ratio) CH2Cb- methanol mixture showed that reaction was completed within 15 minutes. Eventually, the reaction mixture was diluted with methylene chloride and extracted with water. The organic layer was dried over anhydrous MgSO4, filtered, concentrated and, in order to ensure full DMF removal, dried under high vacuum. The resulting crystalline crude material was purified by column chromatography (90 g silica gel, elution with 200 ml of a ChkCVmethanol mixture (volume ratio progressively ranging from 99:1 to 96:4). The desired product (409 mg) was obtained with a 73% yield.
EXAMPLES 5 to 7 - preparation of 4-(2-[(tert-butoxycarbonyl)(methyl)aminol- 1 -hvdroxyethvDphenyl isobutyrate: 4-(2-r(te/t-butoxycarbonyl)(methyl)aminol- 1 -hvdroxyethvDphenyl hexanoate; and 4-(2-[(te/t-butoxycarbonyl)(methyl)- aminol-1 -hvdroxyethvDphenyl 1 -naphthoate
A flask containing a stirring bar was purged with nitrogen and charged with N-Boc synephrine (obtained in example 2). The flask was fitted with a rubber septum and placed under nitrogen pressure. Dry methylene chloride (10 ml) and triethyl amine (1.05 molar equivalents) were added. Once dissolution was complete, the flask containing the slightly turbid solution was immersed in an ice bath. After sufficient cooling, the appropriate acyl chloride (1 molar equivalent; for the purpose of the example respectively isobutyryl chloride, hexanoyl chloride and 1-naphthoyl chloride) was added dropwise to the stirred solution. Once addition was complete, the ice bath was removed after several minutes, and the clear solution was stirred at room temperature. The progress of the reaction was monitored by TLC on silica using a mixture of CH2Cb and MeOH at 98/2 (v/v). After completion of the reaction was noted, the reaction solution was diluted with methylene chloride, and the resulting solution was extracted first with water and then saturated NaCI. The organic phase was dried over MgSO4, filtered and concentrated on the rotary evaporator. The crude material was purified by silica gel column chromatography eluting the final compound with 98/2, CH2CI2/MeOH (v/v). In this way the following compounds were obtained:
- 4-{2-[(te/t-butoxycarbonyl)(methyl)amino]-1-hydroxyethyl}phenyl isobutyrate (example 5) in 92% yield; - 4-{2-[(tert-butoxycarbonyl)(methyl)amino]-1-hydroxyethyl}phenyl hexanoate (example 6) in 82% yield; and
- 4-{2-[(tert-butoxycarbonyl)(methyl)amino]-1 -hydroxyethyljphenyl 1 - naphthoate (example 7) in 89% yield.
Example 8 - synthesis of 1-r4-(benzoyloxy)phenyll-2-[(te/t-butoxycarbonyl)- methylaminolethyl-1 H-imidazole-1 -carboxylate
The following refers in general to the preparation of N-protected synephrine derivatives according to scheme 1 , step d.
2-[4-(benzoyloxy)phenyl]-2-hydroxy-1-[N-(terf-butoxycarbonyl)- methylamino]ethyl (50 mg, 0.135 mmol) was weighed into a flask equipped with a stirring bar, and the system was purged with nitrogen. Dry methylene chloride (1 ml) was added, and the mixture was stirred until a solution was obtained. To this solution, at room temperature, was added 1 ,1 '- carbonyldiimidazole (hereinafter referred as CDI, 23 mg, 0.142 mmol). Reaction progress was monitored by TLC analysis. Additional portions of CDI were introduced after stirring for 3 hours (6.5 mg, 0.04 mmol), 4.5 hours (6 mg, 0.037 mmol) and 6.5 hours (3.5 mg, 0.022 mmol). After 7.5 hours, the reaction solution was diluted with methylene chloride, and the resulting solution was extracted two times with water. The organic layer was dried over anhydrous MgSO4, filtered and concentrated under reduced pressure, and the residue was dried in vacuo. The desired product was obtained quantitatively (yield: 100 %).
EXAMPLES 9 to 11 - preparation of 1-f4-(isobutanoyloxy)phenyll-2-[(ter/- butoxycarbonyl)-methylamino1ethyl-1 H-imidazole-1 -carboxylate. 1-r4-(hexanoyloxy)phenyl1-2-f(te/t-butoxycarbonyl)-methylaminolethyl-1 H- imidazole-1 -carboxylate and 1 -f4-(naphthoyloxy)phenyll-2-r(te/t-butoxy- carbonyl)-methylaminolethyl-1 H-imidazole-1 -carboxylate
The synthesis of 1-[4-(isobutanoyloxy)phenyl]-2-[(terf-butoxycarbonyl)- methylamino]ethyl-1 H-imidazole-1 -carboxylate (example 9), 1-[4-(hexanoyloxy)phenyl]-2-[(te/t-butoxycarbonyl)-methylamino]ethyl-1 H- imidazole-1-carboxylate (example 10) and 1-[4-(naphthoyloxy)phenyl]-2-[(te/t- butoxycarbonyl)-methylamino]ethyl-1 H-imidazole-1 -carboxylate (example 11 ) was carried out as described in example 8, starting from the compounds of examples 5 to 7 respectively. The title products were all obtained in quantitative yield (higher than 98 %).
EXAMPLE 12 - preparation of 4-M-(acetyloxy)-2-(methylamino)ethvHphenyl acetate hydrochloride The following refers to the preparation of di-O-acyLsynephrine salts according to scheme 1 , step f. A compound obtained according to example 2 (0.246 mmol) was dissolved in 1 ml of 4M HCI in dioxane, and the resulting solution was stirred at room temperature for 1 hour. TLC analysis (performed with a 98:2 (volume ratio) ChbCVmethanol mixture) after one hour indicated complete disappearance of the starting material. The solution was then diluted with ethyl ether, and the resulting cloudy solution was purged with N2 in order to remove HCI. Upon standing 1 hour at room temperature the reaction solution became clear and product white beads deposited. Ether washing was repeated four times. The resulting desired product was dried under vacuum and obtained (60 mg) in a 85% yield.
EXAMPLE 13 - biological evaluation with pE-selectine-Luc transfected cells. L929sA cells were cultured in DMEM supplemented with 5 % new-born calf serum and 5 % fetal calf serum, 100 units/ml penicillin and 0.1 mg/ml streptomycin. L929sA mouse fibroblast cells were stably transfected with pE- selectine-Luc (also referred to as pELAM-luc) by the calcium phosphate precipitation procedure described by De Bosscher et al. in Proc. Natl. Acad. Sci. USA (1997) 94:13504-13509. The co-transfected plasmid pPGKβGeobpA, conferring resistance to G418 and expressing constitutive β- galactosidase enzymatic activity, was used as an internal control. L929sA cells were transiently transfected by the DEAE-dextran transfection method described by De Bosscher et al. (cited supra). Recombinant murine tumor necrosis factor (TNF) was produced according to a method standard in the art. Dexamethasone (hereinafter abbreviated as DEX) commercially available from Sigma, and 2-(4-acetoxyphenyl)-2-chloro- N-methyl-ethylammonium chloride (hereinafter abbreviated as compound A) was synthesized according to Louw et al. in Biochemical Pharmacology (1997) 53:189-197). A stock solution was prepared in ethanol (for DEX) or DMSO (for both comparative compound A and for the compound of example 6 according to this invention, i.e. 1-[4-(benzoyloxy)phenyl]-2-[(tert-butoxy- carbonyl)-methylamino]ethyl-1 H-imidazole-1-carboxylate), aliquoted and stored at -700C. Control experiments verified that the final concentration of organic solvent did not interfere with any of the assays.
Induction was performed in triplicate for each independent experiment, which was carried out at least twice. Induction with DEX, compound A1 and for the compound of example 6 according to this invention at 1 μM, 10 μM or respectively any other indicated concentration were performed at - 2 hours for a total of 8 hours, while TNF (2000 IU/ml) was added at time point zero and left on the cells for 6 hours. After induction, cells were lysed with a lysis buffer (commercially available from Tropix, Bedford, Massachussets) and samples were assayed according to the manufacturer's instructions (Promega Biotech). Promoter activities are expressed as a ratio of luciferase over β- galactosidase, multiplied by 100.
In order to investigate whether the inhibitory effect of compound A or the compound of example 6 according to this invention is directed at the transcriptional level of NF-κB-driven genes, the NF-κB-dependent physiological promoter construct, pE-selectin-Luc stably integrated into L929sA cells, was tested. Inhibition of TNF-induced gene expression by the mediation of the compound of example 6 according to this invention was observed in a dose-responsive manner, as shown in figure 1 B. DEX-mediated and A-mediated inhibition of TNF-induced gene expression were used as controls (figure 1A). In the appended figures, NI stands for non-induced (either in presence of solvent controls like ethanol or DMSO). EXAMPLE 14 - biological evaluation with p(IL6-kB)r50hu.ll_6P-luc+ transfected cells
L929sA mouse fibroblast cells were cultured in DMEM supplemented with 5% newborn calf serum and 5% FCS, 100 units/ml penicillin and 0.1 mg/ml streptomycin. The L929sA mouse fibroblast cells were stably transfected with plasmid p(IL6-kB)3-50hu.ll_6P-luc+ by a calcium phosphate precipitation procedure wel known in the art. The co-transfected plasmid pPGKβGeobpA, conferring resistance to G418 and expressing constitutive b- galactosidase enzymatic activity, was used as an internal control. TNF, Dexamethasone, and compound A were obtained and handled as described for example 13.
Inductions were performed in triplicate for each independent experiment, which was carried out at least twice. Inductions with DEX, compound A or synephrine derivatives of the present invention at 1mM, 1OmM or at the indicated concentrations respectively, were performed at -2 hours for a total of 8 hours, while TNF (20001 U/ml) was added at time point zero and left on the cells for 6 hours. Synephrine derivatives tested according to this protocol included 1-[4-(isobutanoyloxy)phenyl]-2-[(ferNbutoxycarbonyl)-methyl-amino]- ethyl-1 H-imidazole-1-carboxylate, and 1-[4-(naphthoyloxy)phenyl]-2-[(fe/t- butoxycarbonyl)-methylamino]ethyl-1 H-imidazole-1 -carboxylate.
After induction with TNF1 cells were lysed with a lysis buffer (commercially available from TROPIX, Bedford, Massachussets) and samples were assayed for their protein or β-galactosidase content and luciferase activity according to the manufacturer's instructions (Promega Biotech). Promoter activities are calculated as ratios of luciferase over β-galactosidase and represented as ' induction fold ', whereby the promoter activity of the solvent-treated fraction was arbitrarily taken as 1.
In order to demonstrate that these synephrine derivatives are antiinflammatory agents, and that their mechanism of action is directed at the transcriptional level of NF-kB-driven genes (with NF-kB being widely acknowledged as a key regulatory transcription factor driving inflammatory cytokine gene expression), we tested the recombinant NF-kB-driven promoter construct p(IL6-kB)3-50hu.lL6P-luc+, stably integrated into L929sA cells, and observed for specific and selected synephrine derivatives an inhibition of the pro-inflammatory TNF-induced gene expression in a dose-responsive manner. Figure 2 illustrates the anti-inflammatory effect of 1-[4-(naphthoyloxy)- phenyll^-Kte/t-butoxycarbonylJ-methylaminolethyl-I H-imidazole-i-carboxy- late (referred to in figure 2 as Naphth). Figure 3 illustrates the antiinflammatory effect of 1-[4-(isobutanoyloxy)phenyl]-2-[(fe/t-butoxycarbonyl)- methylamino]ethyl-1 H-imidazole-1-carboxylate (referred to in figure 3 as Isobut). Dexamethasone and compound A (referred to in figure 2 and 3 as DEX and CpdA respectively) were used as positive control based on their known anti-inflammatory effect. As a negative control, solvent control (solvent Ctrl) was performed as well.
It was thus observed that the synephrine derivatives of this invention display a marked anti-inflammatory potential. The anti-inflammatory effectiveness of the active compounds are comparable to the effectiveness obtained by using known anti-inflammatory compounds such as dexamethasone or compound A.

Claims

1. A compound represented by the structural formula (I):
wherein: - Ri is -C(=O)-R4 or -S(=O)2-R4,
- R2 is -C(=O)-R6,
- R3 is hydrogen, -C(=O)-R7l -C(=O)-OR7 or aryl-Ci-7 alkyl;
- R4 is selected from the group consisting of R5, -OR5, -NHR5 and -SR5,
- R5 is selected from the group consisting of hydrogen, C2-io alkyl, C3-I0 cycloalkyl, C2-i0 alkenyl, C2-i0 alkynyl, aryl, aryl-Ci-7 alkyl, and saturated, partly unsaturated or aromatic heterocyclic groups,
- R6 is selected from the group consisting of C2-I0 alkyl, C3-10 cycloalkyl, C2-10 alkenyl, C2-10 alkynyl, aryl, arylalkyl, and saturated, partly unsaturated or aromatic heterocyclic groups, - R7 is selected from the group consisting of C1-I0 alkyl, C2-10 alkenyl, aryl and alkyl, wherein each of said alkyl or aryl groups may be substituted with one or more substituents independently selected from the group consisting of halogen, alkyl, alkoxy, nitro, cyano and hydroxy, a stereoisomer thereof, a solvate thereof, or a salt thereof.
2. A compound according to claim 1 , wherein R1 is -C(=O)-R4, and R4 is selected from R5. .
3. A compound according to claim 1 or claim 2, wherein R1 is -C(=O)-R4, and R4 is selected from R5, and Ri is the same as R2.
4. A compound according to any of claims 1 to 3, wherein R1 is selected from the group consisting of benzoyl, p-toluoyl, 1-naphthalenecarbonyl, 2- naphthalenecarbonyl, 4-morpholinocarbonyl, 1-piperidinocarbonyl, 1- imidazolidinocarbonyl, 1-pyrrolidinocarbonyl, 2-thiazolecarbonyl, 1-methyl-1 H- pyrrole-2-carbonyl, 2-furanecarbonyl, 3-furanecarbonyl, 3-pyridinecarbonyl, 4- pyridinecarbonyl, 2-thiophenecarbonyl, cyclobutanecarbonyl, cyclopentane- carbonyl, cyclohexanecarbonyl, 1-adamantanecarbonyl, pipecolinyl and 2- norbornanecarbonyl.
5. A compound according to claim 1 or claim 2, wherein Ri is selected from the group consisting of acetyl, formyl, propanoyl, butanoyl and pentanoyl.
6. A compound according to any of claims 1 to 5, wherein R3 is the same as R2.
7. A compound according to any of claims 1 to 6, wherein R3 is selected from the group consisting of arylcarbonyl, alkyloxycarbonyl and arylalkyloxycarbonyl.
8. A compound according to any of claims 1 to 7, wherein R3 is tert- butoxycarbonyl.
9. A non-toxic acid addition salt of a compound according to any of claims 1 to 8 wherein R3 is hydrogen.
10. A method for preparing a compound according to any of claims 1 to 9, comprising the steps of:
(a) reacting synephrine with an amino-protecting reagent to form an amino- protected synephrine,
(b) reacting said amino-protected synephrine with a chloride selected from the group consisting of carboxylic acid chlorides, carbamic acid chlorides, chloroformates, thiocarboxylic acid chlorides, imidic acid chlorides and sulfonic acid chlorides to produce a 4-[2-(N-protected-methylamino)-1- hydroxyethyl] phenyl ester, and (c) reacting said 4-[2-(N-protected-methylamino)-1-hydroxyethyl]phenyl ester with an activated carbonyl compound selected from the group consisting of carboxylic acid chlorides, carbamic acid chlorides, chloroformates, thiocarboxylic acid chlorides, imidic acid chlorides, 1 ,1 '- carbonyldiimidazole and 1 ,1 '-carbonylditriazole.
11. A method according to claim 10, wherein step (a) comprises reacting synephrine with an amino-protected thiazolidine-2-thione.
12. A method according to claim 11 , wherein the amino-protected thiazolidine- 2-thione used in step (a) is te/t-butoxycarbonyl-thiazolidine-2-thione and step (a) results into a fe/t-butoxycarbonyl-protected synephrine.
13. A method according to any of claims 10 to 12, wherein said N-protected synephrine is reacted in step (b) with a carboxylic acid chloride.
14. A method according to any of claims 10 to 13, further comprising the step
(d) of selectively de-protecting the amino group of the compound resulting from step (c), without affecting any of groups Ri and R2.
15. A method according to claim 14, wherein said step (d) simultaneously achieves the formation of a non-toxic acid addition salt.
16. A pharmaceutical composition comprising a therapeutic effective amount of a compound according to any of claims 1 to 9, and optionally one or more pharmaceutically acceptable carriers.
17. A pharmaceutical composition according to claim 16, further comprising a therapeutic amount of one or more anti-inflammatory drugs.
18. Use of a compound according to any of claims 1 to 9 for the manufacture of a medicament for preventing or treating an inflammatory disease or disorder.
19. A method of ameliorating or preventing or treating an inflammatory disease or disorder, comprising administration of a synephrine derivative according to any of claims 1 to 9 or a synephrine derivative manufactured by a process according to any of claims 10 to 15 or a composition according to claim 16 or 17 to a patient in need thereof.
20. A compound according to claim 1 , wherein when R4 is R5 and R1 is - C(=O)-R4 then a heterocyclic group R5 is attached through one of its heteroatoms to the carbon atom of the carbonyl group of R1.
21. A compound according to claim 1 , wherein a heterocyclic group RQ is attached through one of its heteroatoms to the carbon atom of the carbonyl group of R2.
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JP2009524588A (en) 2009-07-02
AU2006328912A1 (en) 2007-06-28
US20090029999A1 (en) 2009-01-29
GB0526123D0 (en) 2006-02-01
CA2634359A1 (en) 2007-06-28
US8039501B2 (en) 2011-10-18
WO2007071452A1 (en) 2007-06-28

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